Canonical Allele Identifier: CA1624303961

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961292T= , CM000668.2:g.42961292T=	GRCh38
NC_000006.11:g.42929030T= , CM000668.1:g.42929030T=	GRCh37
NC_000006.10:g.43037008T=	NCBI36
NG_008396.1:g.5531T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+319T= MANE Select	ENSP00000361894.3:n.206+319T=
ENST00000372808.3:c.206+319T=	ENSP00000361894.3:n.206+319T=
NM_018960.4:c.206+319T=	NP_061833.1:n.206+319T=
XM_011514493.1:c.-13-920T=	XP_011512795.1:n.-13-920T=
XM_011514494.1:c.-13-920T=	XP_011512796.1:n.-13-920T=
NM_001318856.1:c.9-920T=	NP_001305785.1:n.9-920T=
NM_001318857.1:c.152-1470T=	NP_001305786.1:n.152-1470T=
NM_001318858.1:c.152-1470T=	NP_001305787.1:n.152-1470T=
NM_001318865.1:c.206+319T=	NP_001305794.1:n.206+319T=
NM_018960.5:c.206+319T=	NP_061833.1:n.206+319T=
NR_134890.1:n.690-1470T=
NR_134891.1:n.593-1470T=
NR_134892.1:n.593-920T=
NR_134899.1:n.220+319T=
NM_018960.6:c.206+319T= MANE Select	NP_061833.1:n.206+319T=
NM_001318856.2:c.9-920T=	NP_001305785.1:n.9-920T=
NM_001318857.2:c.152-1470T=	NP_001305786.1:n.152-1470T=
NM_001318858.2:c.152-1470T=	NP_001305787.1:n.152-1470T=
NM_001318865.2:c.206+319T=	NP_001305794.1:n.206+319T=
NR_134890.2:n.340-1470T=
NR_134891.2:n.243-1470T=
NR_134892.2:n.243-920T=
NR_134899.2:n.220+319T=