Canonical Allele Identifier: CA2317699070

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399063T= , CM000681.2:g.1399063T=	GRCh38
NC_000019.9:g.1399062T= , CM000681.1:g.1399062T=	GRCh37
NC_000019.8:g.1350062T=	NCBI36
NG_009785.1:g.7491A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.460-37A= MANE Select	ENSP00000252288.1:n.460-37A=
ENST00000447102.8:c.460-37A=	ENSP00000403536.2:n.460-37A=
ENST00000591788.3:c.143-37A=
ENST00000640164.1:n.293-37A=
ENST00000640762.1:c.391-37A=	ENSP00000492031.1:n.391-37A=
ENST00000252288.6:c.460-37A=	ENSP00000252288.1:n.460-37A=
ENST00000447102.7:c.460-37A=	ENSP00000403536.2:n.460-37A=
ENST00000591788.2:c.145-37A=	ENSP00000466341.2:n.145-37A=
NM_000156.5:c.460-37A=	NP_000147.1:n.460-37A=
NM_138924.2:c.460-37A=	NP_620279.1:n.460-37A=
NM_000156.6:c.460-37A= MANE Select	NP_000147.1:n.460-37A=
NM_138924.3:c.460-37A=	NP_620279.1:n.460-37A=