Canonical Allele Identifier: CA1624303671

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42961012G= , CM000668.2:g.42961012G=	GRCh38
NC_000006.11:g.42928750G= , CM000668.1:g.42928750G=	GRCh37
NC_000006.10:g.43036728G=	NCBI36
NG_008396.1:g.5251G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.206+39G= MANE Select	ENSP00000361894.3:n.206+39G=
ENST00000372808.3:c.206+39G=	ENSP00000361894.3:n.206+39G=
NM_018960.4:c.206+39G=	NP_061833.1:n.206+39G=
XM_011514493.1:c.-13-1200G=	XP_011512795.1:n.-13-1200G=
XM_011514494.1:c.-13-1200G=	XP_011512796.1:n.-13-1200G=
NM_001318856.1:c.9-1200G=	NP_001305785.1:n.9-1200G=
NM_001318857.1:c.152-1750G=	NP_001305786.1:n.152-1750G=
NM_001318858.1:c.152-1750G=	NP_001305787.1:n.152-1750G=
NM_001318865.1:c.206+39G=	NP_001305794.1:n.206+39G=
NM_018960.5:c.206+39G=	NP_061833.1:n.206+39G=
NR_134890.1:n.690-1750G=
NR_134891.1:n.593-1750G=
NR_134892.1:n.593-1200G=
NR_134899.1:n.220+39G=
NM_018960.6:c.206+39G= MANE Select	NP_061833.1:n.206+39G=
NM_001318856.2:c.9-1200G=	NP_001305785.1:n.9-1200G=
NM_001318857.2:c.152-1750G=	NP_001305786.1:n.152-1750G=
NM_001318858.2:c.152-1750G=	NP_001305787.1:n.152-1750G=
NM_001318865.2:c.206+39G=	NP_001305794.1:n.206+39G=
NR_134890.2:n.340-1750G=
NR_134891.2:n.243-1750G=
NR_134892.2:n.243-1200G=
NR_134899.2:n.220+39G=