Canonical Allele Identifier: CA2317699028
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398993C= , CM000681.2:g.1398993C= GRCh38
NC_000019.9:g.1398992C= , CM000681.1:g.1398992C= GRCh37
NC_000019.8:g.1349992C= NCBI36
NG_009785.1:g.7561G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.493G= MANE Select ENSP00000252288.1:p.Val165=
ENST00000447102.8:c.493G= ENSP00000403536.2:p.Val165=
ENST00000591788.3:c.176G=
ENST00000640164.1:n.326G=
ENST00000640762.1:c.424G= ENSP00000492031.1:p.Val142=
ENST00000252288.6:c.493G= ENSP00000252288.1:p.Val165=
ENST00000447102.7:c.493G= ENSP00000403536.2:p.Val165=
ENST00000591788.2:c.178G= ENSP00000466341.2:p.Val60=
NM_000156.5:c.493G= NP_000147.1:p.Val165=
NM_138924.2:c.493G= NP_620279.1:p.Val165=
NM_000156.6:c.493G= MANE Select NP_000147.1:p.Val165=
NM_138924.3:c.493G= NP_620279.1:p.Val165=