Canonical Allele Identifier: CA009240

Gene: MEN1

Linked Data

• MyVariant Identifiers: chr11:g.64572018T>T (hg19) ; chr11:g.64804546T>T (hg38)
• PubMed: PMID:564891 ; PMID:9215689 ; PMID:18775714 ; PMID:22703879

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64804546T= , CM000673.2:g.64804546T=	GRCh38
NC_000011.9:g.64572018T= , CM000673.1:g.64572018T=	GRCh37
NC_000011.8:g.64328594T=	NCBI36
NG_033040.1:g.3696A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377313.7:c.1636A=	ENSP00000366530.1:p.Thr546=
ENST00000394374.8:c.*929A=	ENSP00000377899.4:n.*929A=
ENST00000394376.7:c.1612A=	ENSP00000377901.3:p.Thr538=
ENST00000413626.2:c.1621A=	ENSP00000411218.2:p.Thr541=
ENST00000424912.2:c.1621A=	ENSP00000388016.2:p.Thr541=
ENST00000429702.6:c.1621A=	ENSP00000402752.2:p.Thr541=
ENST00000672079.2:c.*717A=	ENSP00000500905.2:n.*717A=
ENST00000710881.1:c.1636A=	ENSP00000518530.1:p.Thr546=
ENST00000394376.6:c.963A=
ENST00000478548.3:n.2114A=
ENST00000671939.2:n.1583A=
ENST00000671965.2:n.2003A=
ENST00000312049.11:c.1621A=	ENSP00000308975.6:p.Thr541=
ENST00000315422.9:c.1621A=	ENSP00000323747.4:p.Thr541=
ENST00000377313.6:c.1636A=	ENSP00000366530.1:p.Thr546=
ENST00000440873.6:c.1621A=	ENSP00000413944.2:p.Thr541=
ENST00000450708.7:c.1621A= MANE Select	ENSP00000394933.3:p.Thr541=
ENST00000478548.2:n.2122A=
ENST00000671939.1:n.1898A=
ENST00000672304.1:c.1747A=	ENSP00000500585.1:p.Thr583=
ENST00000312049.10:c.1621A=	ENSP00000308975.6:p.Thr541=
ENST00000315422.8:c.1621A=	ENSP00000323747.4:p.Thr541=
ENST00000337652.5:c.1636A=	ENSP00000337088.1:p.Thr546=
ENST00000377313.5:c.1636A=	ENSP00000366530.1:p.Thr546=
ENST00000377316.6:c.1456A=	ENSP00000366533.1:p.Thr486=
ENST00000377321.5:c.1516A=	ENSP00000366538.1:p.Thr506=
ENST00000377326.7:c.1621A=	ENSP00000366543.3:p.Thr541=
ENST00000394374.6:c.1636A=	ENSP00000377899.2:p.Thr546=
ENST00000394376.5:c.1636A=	ENSP00000377901.1:p.Thr546=
ENST00000478548.1:n.1170A=
XM_005274001.3:c.1621A=	XP_005274058.1:p.Thr541=
XM_011545040.1:c.1747A=	XP_011543342.1:p.Thr583=
XM_011545041.1:c.1747A=	XP_011543343.1:p.Thr583=
XM_011545042.1:c.1747A=	XP_011543344.1:p.Thr583=
XM_005274001.4:c.1621A=	XP_005274058.1:p.Thr541=
XM_011545041.2:c.1747A=	XP_011543343.1:p.Thr583=
XM_011545042.3:c.1747A=	XP_011543344.1:p.Thr583=
XM_017017765.1:c.1762A=	XP_016873254.1:p.Thr588=
XM_017017766.1:c.1762A=	XP_016873255.1:p.Thr588=
XM_017017767.2:c.1762A=	XP_016873256.1:p.Thr588=
XM_017017768.1:c.1762A=	XP_016873257.1:p.Thr588=
XM_017017769.1:c.1621A=	XP_016873258.1:p.Thr541=
XM_017017770.2:c.1621A=	XP_016873259.1:p.Thr541=
NM_001370259.2:c.1621A= MANE Select	NP_001357188.2:p.Thr541=
NM_000244.4:c.1636A=	NP_000235.3:p.Thr546=
NM_001370251.2:c.1747A=	NP_001357180.2:p.Thr583=
NM_001370260.2:c.1621A=	NP_001357189.2:p.Thr541=
NM_001370261.2:c.1621A=	NP_001357190.2:p.Thr541=
NM_001370262.2:c.1516A=	NP_001357191.2:p.Thr506=
NM_001370263.2:c.1516A=	NP_001357192.2:p.Thr506=
NM_130799.3:c.1621A=	NP_570711.2:p.Thr541=
NM_130800.3:c.1636A=	NP_570712.2:p.Thr546=
NM_130801.3:c.1636A=	NP_570713.2:p.Thr546=
NM_130802.3:c.1636A=	NP_570714.2:p.Thr546=
NM_130803.3:c.1636A=	NP_570715.2:p.Thr546=
NM_130804.3:c.1636A=	NP_570716.2:p.Thr546=