Canonical Allele Identifier: CA1978892590

Gene: MEN1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64807892_64807901delinsCGCTCAGCCA , CM000673.2:g.64807892_64807901delinsCGCTCAGCCA	GRCh38
NC_000011.9:g.64575364_64575373delinsCGCTCAGCCA , CM000673.1:g.64575364_64575373delinsCGCTCAGCCA	GRCh37
NC_000011.8:g.64331940_64331949delinsCGCTCAGCCA	NCBI36
NG_008929.1:g.8394_8403delinsTGGCTGAGCG , LRG_509:g.8394_8403delinsTGGCTGAGCG
NG_033040.1:g.341_350delinsTGGCTGAGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000377313.7:c.659_668delinsTGGCTGAGCG	ENSP00000366530.1:p.Val220=
ENST00000394374.8:c.640+4_640+13delinsTGGCTGAGCG	ENSP00000377899.4:n.640+4_640+13delinsTGG...
ENST00000394376.7:c.644_653delinsTGGCTGAGCG	ENSP00000377901.3:p.Val215=
ENST00000413626.2:c.644_653delinsTGGCTGAGCG	ENSP00000411218.2:p.Val215=
ENST00000424912.2:c.644_653delinsTGGCTGAGCG	ENSP00000388016.2:p.Val215=
ENST00000429702.6:c.644_653delinsTGGCTGAGCG	ENSP00000402752.2:p.Val215=
ENST00000672079.2:c.644_653delinsTGGCTGAGCG	ENSP00000500905.2:p.Val215=
ENST00000710881.1:c.659_668delinsTGGCTGAGCG	ENSP00000518530.1:p.Val220=
ENST00000394374.7:c.401+4_401+13delinsTGGCTGAGCG
ENST00000478548.3:n.676_685delinsTGGCTGAGCG
ENST00000671939.2:n.396_405delinsTGGCTGAGCG
ENST00000671965.2:n.304_313delinsTGGCTGAGCG
ENST00000312049.11:c.644_653delinsTGGCTGAGCG	ENSP00000308975.6:p.Val215=
ENST00000315422.9:c.644_653delinsTGGCTGAGCG	ENSP00000323747.4:p.Val215=
ENST00000377313.6:c.659_668delinsTGGCTGAGCG	ENSP00000366530.1:p.Val220=
ENST00000440873.6:c.644_653delinsTGGCTGAGCG	ENSP00000413944.2:p.Val215=
ENST00000450708.7:c.644_653delinsTGGCTGAGCG MANE Select	ENSP00000394933.3:p.Val215=
ENST00000478548.2:n.684_693delinsTGGCTGAGCG
ENST00000671939.1:n.711_720delinsTGGCTGAGCG
ENST00000671965.1:n.304_313delinsTGGCTGAGCG
ENST00000672079.1:c.370_379delinsTGGCTGAGCG
ENST00000672304.1:c.644_653delinsTGGCTGAGCG	ENSP00000500585.1:p.Val215=
ENST00000312049.10:c.644_653delinsTGGCTGAGCG	ENSP00000308975.6:p.Val215=
ENST00000315422.8:c.644_653delinsTGGCTGAGCG	ENSP00000323747.4:p.Val215=
ENST00000337652.5:c.659_668delinsTGGCTGAGCG	ENSP00000337088.1:p.Val220=
ENST00000377313.5:c.659_668delinsTGGCTGAGCG	ENSP00000366530.1:p.Val220=
ENST00000377316.6:c.644_653delinsTGGCTGAGCG	ENSP00000366533.1:p.Val215=
ENST00000377321.5:c.549+95_549+104delinsTGGCTGAGCG	ENSP00000366538.1:n.549+95_549+104delinsT...
ENST00000377326.7:c.644_653delinsTGGCTGAGCG	ENSP00000366543.3:p.Val215=
ENST00000394374.6:c.659_668delinsTGGCTGAGCG	ENSP00000377899.2:p.Val220=
ENST00000394376.5:c.659_668delinsTGGCTGAGCG	ENSP00000377901.1:p.Val220=
ENST00000413626.1:c.644_653delinsTGGCTGAGCG	ENSP00000411218.1:p.Val215=
ENST00000440873.5:c.644_653delinsTGGCTGAGCG	ENSP00000413944.1:p.Val215=
ENST00000450708.5:c.644_653delinsTGGCTGAGCG	ENSP00000394933.1:p.Val215=
NM_000244.3:c.659_668delinsTGGCTGAGCG , LRG_509t1:c.659_668delinsTGGCTGAGCG	NP_000235.2:p.Val220=
NM_130799.2:c.644_653delinsTGGCTGAGCG , LRG_509t2:c.644_653delinsTGGCTGAGCG	NP_570711.1:p.Val215=
NM_130800.2:c.659_668delinsTGGCTGAGCG	NP_570712.1:p.Val220=
NM_130801.2:c.659_668delinsTGGCTGAGCG	NP_570713.1:p.Val220=
NM_130802.2:c.659_668delinsTGGCTGAGCG	NP_570714.1:p.Val220=
NM_130803.2:c.659_668delinsTGGCTGAGCG	NP_570715.1:p.Val220=
NM_130804.2:c.659_668delinsTGGCTGAGCG	NP_570716.1:p.Val220=
XM_005274001.3:c.644_653delinsTGGCTGAGCG	XP_005274058.1:p.Val215=
XM_011545040.1:c.644_653delinsTGGCTGAGCG	XP_011543342.1:p.Val215=
XM_011545041.1:c.644_653delinsTGGCTGAGCG	XP_011543343.1:p.Val215=
XM_011545042.1:c.644_653delinsTGGCTGAGCG	XP_011543344.1:p.Val215=
XM_005274001.4:c.644_653delinsTGGCTGAGCG	XP_005274058.1:p.Val215=
XM_011545041.2:c.644_653delinsTGGCTGAGCG	XP_011543343.1:p.Val215=
XM_011545042.3:c.644_653delinsTGGCTGAGCG	XP_011543344.1:p.Val215=
XM_017017765.1:c.659_668delinsTGGCTGAGCG	XP_016873254.1:p.Val220=
XM_017017766.1:c.659_668delinsTGGCTGAGCG	XP_016873255.1:p.Val220=
XM_017017767.2:c.659_668delinsTGGCTGAGCG	XP_016873256.1:p.Val220=
XM_017017768.1:c.659_668delinsTGGCTGAGCG	XP_016873257.1:p.Val220=
XM_017017769.1:c.644_653delinsTGGCTGAGCG	XP_016873258.1:p.Val215=
XM_017017770.2:c.644_653delinsTGGCTGAGCG	XP_016873259.1:p.Val215=
NM_001370251.1:c.644_653delinsTGGCTGAGCG	NP_001357180.1:p.Val215=
NM_001370259.2:c.644_653delinsTGGCTGAGCG MANE Select	NP_001357188.2:p.Val215=
NM_001370260.1:c.644_653delinsTGGCTGAGCG	NP_001357189.1:p.Val215=
NM_001370261.1:c.644_653delinsTGGCTGAGCG	NP_001357190.1:p.Val215=
NM_001370262.1:c.549+95_549+104delinsTGGCTGAGCG	NP_001357191.1:n.549+95_549+104delinsTGGC...
NM_001370263.1:c.549+95_549+104delinsTGGCTGAGCG	NP_001357192.1:n.549+95_549+104delinsTGGC...
NM_000244.4:c.659_668delinsTGGCTGAGCG	NP_000235.3:p.Val220=
NM_001370251.2:c.644_653delinsTGGCTGAGCG	NP_001357180.2:p.Val215=
NM_001370260.2:c.644_653delinsTGGCTGAGCG	NP_001357189.2:p.Val215=
NM_001370261.2:c.644_653delinsTGGCTGAGCG	NP_001357190.2:p.Val215=
NM_001370262.2:c.549+95_549+104delinsTGGCTGAGCG	NP_001357191.2:n.549+95_549+104delinsTGGC...
NM_001370263.2:c.549+95_549+104delinsTGGCTGAGCG	NP_001357192.2:n.549+95_549+104delinsTGGC...
NM_130799.3:c.644_653delinsTGGCTGAGCG	NP_570711.2:p.Val215=
NM_130800.3:c.659_668delinsTGGCTGAGCG	NP_570712.2:p.Val220=
NM_130801.3:c.659_668delinsTGGCTGAGCG	NP_570713.2:p.Val220=
NM_130802.3:c.659_668delinsTGGCTGAGCG	NP_570714.2:p.Val220=
NM_130803.3:c.659_668delinsTGGCTGAGCG	NP_570715.2:p.Val220=
NM_130804.3:c.659_668delinsTGGCTGAGCG	NP_570716.2:p.Val220=