Canonical Allele Identifier: CA1624303448

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960893C= , CM000668.2:g.42960893C=	GRCh38
NC_000006.11:g.42928631C= , CM000668.1:g.42928631C=	GRCh37
NC_000006.10:g.43036609C=	NCBI36
NG_008396.1:g.5132C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.126C= MANE Select	ENSP00000361894.3:p.Thr42=
ENST00000372808.3:c.126C=	ENSP00000361894.3:p.Thr42=
NM_018960.4:c.126C=	NP_061833.1:p.Thr42=
XM_011514493.1:c.-13-1319C=	XP_011512795.1:n.-13-1319C=
XM_011514494.1:c.-13-1319C=	XP_011512796.1:n.-13-1319C=
NM_001318856.1:c.9-1319C=	NP_001305785.1:n.9-1319C=
NM_001318857.1:c.152-1869C=	NP_001305786.1:n.152-1869C=
NM_001318858.1:c.152-1869C=	NP_001305787.1:n.152-1869C=
NM_001318865.1:c.126C=	NP_001305794.1:p.Thr42=
NM_018960.5:c.126C=	NP_061833.1:p.Thr42=
NR_134890.1:n.690-1869C=
NR_134891.1:n.593-1869C=
NR_134892.1:n.593-1319C=
NR_134899.1:n.140C=
NM_018960.6:c.126C= MANE Select	NP_061833.1:p.Thr42=
NM_001318856.2:c.9-1319C=	NP_001305785.1:n.9-1319C=
NM_001318857.2:c.152-1869C=	NP_001305786.1:n.152-1869C=
NM_001318858.2:c.152-1869C=	NP_001305787.1:n.152-1869C=
NM_001318865.2:c.126C=	NP_001305794.1:p.Thr42=
NR_134890.2:n.340-1869C=
NR_134891.2:n.243-1869C=
NR_134892.2:n.243-1319C=
NR_134899.2:n.140C=