Canonical Allele Identifier: CA345420935

Gene: CHRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.239907803G>A , CM000663.2:g.239907803G>A	GRCh38
NC_000001.10:g.240071103G>A , CM000663.1:g.240071103G>A	GRCh37
NC_000001.9:g.238137726G>A	NCBI36
NG_032046.1:g.283731G>A
NG_032046.2:g.525874G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001375978.1:c.352G>A MANE Select	NP_001362907.1:p.Gly118Arg
ENST00000676153.1:c.352G>A MANE Select	ENSP00000502667.1:p.Gly118Arg
NM_000740.2:c.352G>A	NP_000731.1:p.Gly118Arg
NM_000740.3:c.352G>A	NP_000731.1:p.Gly118Arg
NM_000740.4:c.352G>A	NP_000731.1:p.Gly118Arg
NM_001347716.1:c.352G>A	NP_001334645.1:p.Gly118Arg
NM_001347716.2:c.352G>A	NP_001334645.1:p.Gly118Arg
NM_001375979.1:c.352G>A	NP_001362908.1:p.Gly118Arg
NM_001375980.1:c.352G>A	NP_001362909.1:p.Gly118Arg
NM_001375981.1:c.352G>A	NP_001362910.1:p.Gly118Arg
NM_001375982.1:c.352G>A	NP_001362911.1:p.Gly118Arg
NM_001375983.1:c.352G>A	NP_001362912.1:p.Gly118Arg
NM_001375984.1:c.352G>A	NP_001362913.1:p.Gly118Arg
NM_001375985.1:c.352G>A	NP_001362914.1:p.Gly118Arg
ENST00000255380.8:c.352G>A	ENSP00000255380.4:p.Gly118Arg
ENST00000615928.4:c.352G>A	ENSP00000482377.1:p.Gly118Arg
ENST00000615928.5:c.352G>A	ENSP00000482377.1:p.Gly118Arg
ENST00000675184.1:c.352G>A	ENSP00000502349.1:p.Gly118Arg
ENST00000675709.1:c.352G>A	ENSP00000502129.1:p.Gly118Arg
ENST00000676433.1:c.352G>A	ENSP00000502013.1:p.Gly118Arg
XM_005273032.2:c.352G>A	XP_005273089.1:p.Gly118Arg
XM_005273032.3:c.352G>A	XP_005273089.1:p.Gly118Arg
XM_005273034.2:c.352G>A	XP_005273091.1:p.Gly118Arg
XM_011544041.1:c.352G>A	XP_011542343.1:p.Gly118Arg
XM_011544041.2:c.352G>A	XP_011542343.1:p.Gly118Arg
XM_011544042.1:c.352G>A	XP_011542344.1:p.Gly118Arg
XM_011544043.1:c.352G>A	XP_011542345.1:p.Gly118Arg
XM_011544043.2:c.352G>A	XP_011542345.1:p.Gly118Arg
XM_011544044.1:c.352G>A	XP_011542346.1:p.Gly118Arg
XM_011544044.2:c.352G>A	XP_011542346.1:p.Gly118Arg
XM_011544045.1:c.352G>A	XP_011542347.1:p.Gly118Arg
XM_011544046.1:c.352G>A	XP_011542348.1:p.Gly118Arg
XM_011544046.2:c.352G>A	XP_011542348.1:p.Gly118Arg
XM_011544047.1:c.352G>A	XP_011542349.1:p.Gly118Arg
XM_011544047.2:c.352G>A	XP_011542349.1:p.Gly118Arg
XM_017000152.2:c.352G>A	XP_016855641.1:p.Gly118Arg
XM_017000153.1:c.352G>A	XP_016855642.1:p.Gly118Arg
XM_017000154.1:c.352G>A	XP_016855643.1:p.Gly118Arg
XM_017000155.1:c.352G>A	XP_016855644.1:p.Gly118Arg
XM_017000156.1:c.352G>A	XP_016855645.1:p.Gly118Arg
XM_017000157.2:c.352G>A	XP_016855646.1:p.Gly118Arg
XM_017000158.1:c.352G>A	XP_016855647.1:p.Gly118Arg
XM_017000159.1:c.352G>A	XP_016855648.1:p.Gly118Arg
XM_017000160.2:c.352G>A	XP_016855649.1:p.Gly118Arg
XM_017000161.1:c.352G>A	XP_016855650.1:p.Gly118Arg
XM_017000162.1:c.352G>A	XP_016855651.1:p.Gly118Arg
XM_017000163.2:c.352G>A	XP_016855652.1:p.Gly118Arg