Canonical Allele Identifier: CA1978892559

Gene: MEN1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64807888_64807896delinsTACCCGCTC , CM000673.2:g.64807888_64807896delinsTACCCGCTC	GRCh38
NC_000011.9:g.64575360_64575368delinsTACCCGCTC , CM000673.1:g.64575360_64575368delinsTACCCGCTC	GRCh37
NC_000011.8:g.64331936_64331944delinsTACCCGCTC	NCBI36
NG_008929.1:g.8399_8407delinsGAGCGGGTA , LRG_509:g.8399_8407delinsGAGCGGGTA
NG_033040.1:g.346_354delinsGAGCGGGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000377313.7:c.664_669+3delinsGAGCGGGTA
ENST00000394374.8:c.640+9_640+17delinsGAGCGGGTA	ENSP00000377899.4:n.640+9_640+17delinsGAG...
ENST00000394376.7:c.649_654+3delinsGAGCGGGTA
ENST00000413626.2:c.649_654+3delinsGAGCGGGTA
ENST00000424912.2:c.649_654+3delinsGAGCGGGTA
ENST00000429702.6:c.649_654+3delinsGAGCGGGTA
ENST00000672079.2:c.649_654+3delinsGAGCGGGTA
ENST00000710881.1:c.664_669+3delinsGAGCGGGTA
ENST00000394374.7:c.401+9_401+17delinsGAGCGGGTA
ENST00000478548.3:n.681_686+3delinsGAGCGGGTA
ENST00000671939.2:n.401_409delinsGAGCGGGTA
ENST00000671965.2:n.309_314+3delinsGAGCGGGTA
ENST00000312049.11:c.649_654+3delinsGAGCGGGTA
ENST00000315422.9:c.649_654+3delinsGAGCGGGTA
ENST00000377313.6:c.664_669+3delinsGAGCGGGTA
ENST00000440873.6:c.649_654+3delinsGAGCGGGTA
ENST00000450708.7:c.649_654+3delinsGAGCGGGTA
ENST00000478548.2:n.689_694+3delinsGAGCGGGTA
ENST00000671939.1:n.716_724delinsGAGCGGGTA
ENST00000671965.1:n.309_314+3delinsGAGCGGGTA
ENST00000672079.1:c.375_380+3delinsGAGCGGGTA
ENST00000672304.1:c.649_654+3delinsGAGCGGGTA
ENST00000312049.10:c.649_654+3delinsGAGCGGGTA
ENST00000315422.8:c.649_654+3delinsGAGCGGGTA
ENST00000337652.5:c.664_669+3delinsGAGCGGGTA
ENST00000377313.5:c.664_669+3delinsGAGCGGGTA
ENST00000377316.6:c.649_654+3delinsGAGCGGGTA
ENST00000377321.5:c.549+100_549+108delinsGAGCGGGTA	ENSP00000366538.1:n.549+100_549+108delins...
ENST00000377326.7:c.649_654+3delinsGAGCGGGTA
ENST00000394374.6:c.664_669+3delinsGAGCGGGTA
ENST00000394376.5:c.664_669+3delinsGAGCGGGTA
ENST00000413626.1:c.649_654+3delinsGAGCGGGTA
ENST00000440873.5:c.649_654+3delinsGAGCGGGTA
ENST00000450708.5:c.649_654+3delinsGAGCGGGTA
NM_000244.3:c.664_669+3delinsGAGCGGGTA , LRG_509t1:c.664_669+3delinsGAGCGGGTA
NM_130799.2:c.649_654+3delinsGAGCGGGTA , LRG_509t2:c.649_654+3delinsGAGCGGGTA
NM_130800.2:c.664_669+3delinsGAGCGGGTA
NM_130801.2:c.664_669+3delinsGAGCGGGTA
NM_130802.2:c.664_669+3delinsGAGCGGGTA
NM_130803.2:c.664_669+3delinsGAGCGGGTA
NM_130804.2:c.664_669+3delinsGAGCGGGTA
XM_005274001.3:c.649_654+3delinsGAGCGGGTA
XM_011545040.1:c.649_654+3delinsGAGCGGGTA
XM_011545041.1:c.649_654+3delinsGAGCGGGTA
XM_011545042.1:c.649_654+3delinsGAGCGGGTA
XM_005274001.4:c.649_654+3delinsGAGCGGGTA
XM_011545041.2:c.649_654+3delinsGAGCGGGTA
XM_011545042.3:c.649_654+3delinsGAGCGGGTA
XM_017017765.1:c.664_669+3delinsGAGCGGGTA
XM_017017766.1:c.664_669+3delinsGAGCGGGTA
XM_017017767.2:c.664_669+3delinsGAGCGGGTA
XM_017017768.1:c.664_669+3delinsGAGCGGGTA
XM_017017769.1:c.649_654+3delinsGAGCGGGTA
XM_017017770.2:c.649_654+3delinsGAGCGGGTA
NM_001370251.1:c.649_654+3delinsGAGCGGGTA
NM_001370259.2:c.649_654+3delinsGAGCGGGTA
NM_001370260.1:c.649_654+3delinsGAGCGGGTA
NM_001370261.1:c.649_654+3delinsGAGCGGGTA
NM_001370262.1:c.549+100_549+108delinsGAGCGGGTA	NP_001357191.1:n.549+100_549+108delinsGAG...
NM_001370263.1:c.549+100_549+108delinsGAGCGGGTA	NP_001357192.1:n.549+100_549+108delinsGAG...
NM_000244.4:c.664_669+3delinsGAGCGGGTA
NM_001370251.2:c.649_654+3delinsGAGCGGGTA
NM_001370260.2:c.649_654+3delinsGAGCGGGTA
NM_001370261.2:c.649_654+3delinsGAGCGGGTA
NM_001370262.2:c.549+100_549+108delinsGAGCGGGTA	NP_001357191.2:n.549+100_549+108delinsGAG...
NM_001370263.2:c.549+100_549+108delinsGAGCGGGTA	NP_001357192.2:n.549+100_549+108delinsGAG...
NM_130799.3:c.649_654+3delinsGAGCGGGTA
NM_130800.3:c.664_669+3delinsGAGCGGGTA
NM_130801.3:c.664_669+3delinsGAGCGGGTA
NM_130802.3:c.664_669+3delinsGAGCGGGTA
NM_130803.3:c.664_669+3delinsGAGCGGGTA
NM_130804.3:c.664_669+3delinsGAGCGGGTA