Canonical Allele Identifier: CA2317698982

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1398899A= , CM000681.2:g.1398899A=	GRCh38
NC_000019.9:g.1398898A= , CM000681.1:g.1398898A=	GRCh37
NC_000019.8:g.1349898A=	NCBI36
NG_009785.1:g.7655T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252288.8:c.570+17T= MANE Select	ENSP00000252288.1:n.570+17T=
ENST00000447102.8:c.587T=	ENSP00000403536.2:p.Val196=
ENST00000591788.3:c.253+17T=
ENST00000640164.1:n.403+17T=
ENST00000640762.1:c.501+17T=	ENSP00000492031.1:n.501+17T=
ENST00000252288.6:c.570+17T=	ENSP00000252288.1:n.570+17T=
ENST00000447102.7:c.587T=	ENSP00000403536.2:p.Val196=
ENST00000591788.2:c.255+17T=	ENSP00000466341.2:n.255+17T=
NM_000156.5:c.570+17T=	NP_000147.1:n.570+17T=
NM_138924.2:c.587T=	NP_620279.1:p.Val196=
NM_000156.6:c.570+17T= MANE Select	NP_000147.1:n.570+17T=
NM_138924.3:c.587T=	NP_620279.1:p.Val196=