Canonical Allele Identifier: CA2317699031

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1398995C= , CM000681.2:g.1398995C=	GRCh38
NC_000019.9:g.1398994C= , CM000681.1:g.1398994C=	GRCh37
NC_000019.8:g.1349994C=	NCBI36
NG_009785.1:g.7559G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000156.6:c.491G= MANE Select	NP_000147.1:p.Gly164=
ENST00000252288.8:c.491G= MANE Select	ENSP00000252288.1:p.Gly164=
NM_000156.5:c.491G=	NP_000147.1:p.Gly164=
NM_138924.2:c.491G=	NP_620279.1:p.Gly164=
NM_138924.3:c.491G=	NP_620279.1:p.Gly164=
ENST00000252288.6:c.491G=	ENSP00000252288.1:p.Gly164=
ENST00000447102.7:c.491G=	ENSP00000403536.2:p.Gly164=
ENST00000447102.8:c.491G=	ENSP00000403536.2:p.Gly164=
ENST00000591788.2:c.176G=	ENSP00000466341.2:p.Gly59=
ENST00000591788.3:c.174G=
ENST00000640164.1:n.324G=
ENST00000640762.1:c.422G=	ENSP00000492031.1:p.Gly141=