Canonical Allele Identifier: CA1624303548

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960936G= , CM000668.2:g.42960936G=	GRCh38
NC_000006.11:g.42928674G= , CM000668.1:g.42928674G=	GRCh37
NC_000006.10:g.43036652G=	NCBI36
NG_008396.1:g.5175G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.169G= MANE Select	ENSP00000361894.3:p.Gly57=
ENST00000372808.3:c.169G=	ENSP00000361894.3:p.Gly57=
NM_018960.4:c.169G=	NP_061833.1:p.Gly57=
XM_011514493.1:c.-13-1276G=	XP_011512795.1:n.-13-1276G=
XM_011514494.1:c.-13-1276G=	XP_011512796.1:n.-13-1276G=
NM_001318856.1:c.9-1276G=	NP_001305785.1:n.9-1276G=
NM_001318857.1:c.152-1826G=	NP_001305786.1:n.152-1826G=
NM_001318858.1:c.152-1826G=	NP_001305787.1:n.152-1826G=
NM_001318865.1:c.169G=	NP_001305794.1:p.Gly57=
NM_018960.5:c.169G=	NP_061833.1:p.Gly57=
NR_134890.1:n.690-1826G=
NR_134891.1:n.593-1826G=
NR_134892.1:n.593-1276G=
NR_134899.1:n.183G=
NM_018960.6:c.169G= MANE Select	NP_061833.1:p.Gly57=
NM_001318856.2:c.9-1276G=	NP_001305785.1:n.9-1276G=
NM_001318857.2:c.152-1826G=	NP_001305786.1:n.152-1826G=
NM_001318858.2:c.152-1826G=	NP_001305787.1:n.152-1826G=
NM_001318865.2:c.169G=	NP_001305794.1:p.Gly57=
NR_134890.2:n.340-1826G=
NR_134891.2:n.243-1826G=
NR_134892.2:n.243-1276G=
NR_134899.2:n.183G=