Canonical Allele Identifier: CA349916

Gene: MEN1

Linked Data

• MyVariant Identifiers: chr11:g.64572557A>A (hg19) ; chr11:g.64805085A>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64805085A= , CM000673.2:g.64805085A=	GRCh38
NC_000011.9:g.64572557A= , CM000673.1:g.64572557A=	GRCh37
NC_000011.8:g.64329133A=	NCBI36
NG_033040.1:g.3157T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377313.7:c.1314T=	ENSP00000366530.1:p.His438=
ENST00000394374.8:c.*607T=	ENSP00000377899.4:n.*607T=
ENST00000394376.7:c.1299T=	ENSP00000377901.3:p.His433=
ENST00000413626.2:c.1299T=	ENSP00000411218.2:p.His433=
ENST00000424912.2:c.1299T=	ENSP00000388016.2:p.His433=
ENST00000429702.6:c.1299T=	ENSP00000402752.2:p.His433=
ENST00000672079.2:c.*395T=	ENSP00000500905.2:n.*395T=
ENST00000710881.1:c.1314T=	ENSP00000518530.1:p.His438=
ENST00000394374.7:c.1046T=
ENST00000394376.6:c.650T=
ENST00000478548.3:n.1792T=
ENST00000671939.2:n.1261T=
ENST00000671965.2:n.1681T=
ENST00000312049.11:c.1299T=	ENSP00000308975.6:p.His433=
ENST00000315422.9:c.1299T=	ENSP00000323747.4:p.His433=
ENST00000377313.6:c.1314T=	ENSP00000366530.1:p.His438=
ENST00000440873.6:c.1299T=	ENSP00000413944.2:p.His433=
ENST00000450708.7:c.1299T= MANE Select	ENSP00000394933.3:p.His433=
ENST00000478548.2:n.1800T=
ENST00000671939.1:n.1576T=
ENST00000672079.1:c.1174T=
ENST00000672304.1:c.1425T=	ENSP00000500585.1:p.His475=
ENST00000312049.10:c.1299T=	ENSP00000308975.6:p.His433=
ENST00000315422.8:c.1299T=	ENSP00000323747.4:p.His433=
ENST00000337652.5:c.1314T=	ENSP00000337088.1:p.His438=
ENST00000377313.5:c.1314T=	ENSP00000366530.1:p.His438=
ENST00000377316.6:c.1186-269T=	ENSP00000366533.1:n.1186-269T=
ENST00000377321.5:c.1194T=	ENSP00000366538.1:p.His398=
ENST00000377326.7:c.1299T=	ENSP00000366543.3:p.His433=
ENST00000394374.6:c.1314T=	ENSP00000377899.2:p.His438=
ENST00000394376.5:c.1314T=	ENSP00000377901.1:p.His438=
ENST00000478548.1:n.848T=
XM_005274001.3:c.1299T=	XP_005274058.1:p.His433=
XM_011545040.1:c.1425T=	XP_011543342.1:p.His475=
XM_011545041.1:c.1425T=	XP_011543343.1:p.His475=
XM_011545042.1:c.1425T=	XP_011543344.1:p.His475=
XM_005274001.4:c.1299T=	XP_005274058.1:p.His433=
XM_011545041.2:c.1425T=	XP_011543343.1:p.His475=
XM_011545042.3:c.1425T=	XP_011543344.1:p.His475=
XM_017017765.1:c.1440T=	XP_016873254.1:p.His480=
XM_017017766.1:c.1440T=	XP_016873255.1:p.His480=
XM_017017767.2:c.1440T=	XP_016873256.1:p.His480=
XM_017017768.1:c.1440T=	XP_016873257.1:p.His480=
XM_017017769.1:c.1299T=	XP_016873258.1:p.His433=
XM_017017770.2:c.1299T=	XP_016873259.1:p.His433=
NM_001370259.2:c.1299T= MANE Select	NP_001357188.2:p.His433=
NM_000244.4:c.1314T=	NP_000235.3:p.His438=
NM_001370251.2:c.1425T=	NP_001357180.2:p.His475=
NM_001370260.2:c.1299T=	NP_001357189.2:p.His433=
NM_001370261.2:c.1299T=	NP_001357190.2:p.His433=
NM_001370262.2:c.1194T=	NP_001357191.2:p.His398=
NM_001370263.2:c.1194T=	NP_001357192.2:p.His398=
NM_130799.3:c.1299T=	NP_570711.2:p.His433=
NM_130800.3:c.1314T=	NP_570712.2:p.His438=
NM_130801.3:c.1314T=	NP_570713.2:p.His438=
NM_130802.3:c.1314T=	NP_570714.2:p.His438=
NM_130803.3:c.1314T=	NP_570715.2:p.His438=
NM_130804.3:c.1314T=	NP_570716.2:p.His438=