Canonical Allele Identifier: CA1745973269

Gene: CHRM2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.137008822T= , CM000669.2:g.137008822T=	GRCh38
NC_000007.13:g.136693569T= , CM000669.1:g.136693569T=	GRCh37
NC_000007.12:g.136344109T=	NCBI36
NG_011846.2:g.145171T= , LRG_405:g.145171T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680005.1:c.-46-5998T= MANE Select	ENSP00000505686.1:n.-46-5998T=
ENST00000320658.9:c.-46-5998T=	ENSP00000319984.5:n.-46-5998T=
ENST00000401861.1:c.-46-5998T=	ENSP00000384401.1:n.-46-5998T=
ENST00000445907.6:c.-46-5998T=	ENSP00000399745.2:n.-46-5998T=
ENST00000453373.5:c.-46-5998T=	ENSP00000415386.1:n.-46-5998T=
NM_000739.2:c.-46-5998T= , LRG_405t1:c.-46-5998T=	NP_000730.1:n.-46-5998T=
NM_001006626.1:c.-46-5998T=	NP_001006627.1:n.-46-5998T=
NM_001006627.1:c.-46-5998T=	NP_001006628.1:n.-46-5998T=
NM_001006628.1:c.-46-5998T=	NP_001006629.1:n.-46-5998T=
NM_001006629.1:c.-46-5998T=	NP_001006630.1:n.-46-5998T=
NM_001006630.1:c.-46-5998T= , LRG_405t2:c.-46-5998T=	NP_001006631.1:n.-46-5998T=
NM_001006631.1:c.-46-5998T=	NP_001006632.1:n.-46-5998T=
NM_001006632.1:c.-46-5998T=	NP_001006633.1:n.-46-5998T=
NR_046103.1:n.341+23972A=
XM_011515769.1:c.-46-5998T=	XP_011514071.1:n.-46-5998T=
XM_011515770.1:c.-46-5998T=	XP_011514072.1:n.-46-5998T=
XM_011515771.1:c.-46-5998T=	XP_011514073.1:n.-46-5998T=
XM_024446648.1:c.-46-5998T=	XP_024302416.1:n.-46-5998T=
NM_001006626.2:c.-46-5998T=	NP_001006627.1:n.-46-5998T=
NM_001006627.2:c.-46-5998T=	NP_001006628.1:n.-46-5998T=
NM_001006628.2:c.-46-5998T=	NP_001006629.1:n.-46-5998T=
NM_001006629.2:c.-46-5998T=	NP_001006630.1:n.-46-5998T=
NM_001006631.2:c.-46-5998T=	NP_001006632.1:n.-46-5998T=
NM_001006632.2:c.-46-5998T=	NP_001006633.1:n.-46-5998T=
NM_000739.3:c.-46-5998T=	NP_000730.1:n.-46-5998T=
NM_001006626.3:c.-46-5998T=	NP_001006627.1:n.-46-5998T=
NM_001006627.3:c.-46-5998T=	NP_001006628.1:n.-46-5998T=
NM_001006628.3:c.-46-5998T=	NP_001006629.1:n.-46-5998T=
NM_001006629.3:c.-46-5998T=	NP_001006630.1:n.-46-5998T=
NM_001006630.2:c.-46-5998T= MANE Select	NP_001006631.1:n.-46-5998T=
NM_001006631.3:c.-46-5998T=	NP_001006632.1:n.-46-5998T=
NM_001006632.3:c.-46-5998T=	NP_001006633.1:n.-46-5998T=
NM_001378972.1:c.-46-5998T=	NP_001365901.1:n.-46-5998T=
NM_001378973.1:c.-46-5998T=	NP_001365902.1:n.-46-5998T=