Canonical Allele Identifier: CA504895137
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1398981G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398982G>A , CM000681.2:g.1398982G>A GRCh38
NC_000019.9:g.1398981G>A , CM000681.1:g.1398981G>A GRCh37
NC_000019.8:g.1349981G>A NCBI36
NG_009785.1:g.7572C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.504C>T MANE Select ENSP00000252288.1:p.Tyr168=
ENST00000447102.8:c.504C>T ENSP00000403536.2:p.Tyr168=
ENST00000591788.3:c.187C>T
ENST00000640164.1:n.337C>T
ENST00000640762.1:c.435C>T ENSP00000492031.1:p.Tyr145=
ENST00000252288.6:c.504C>T ENSP00000252288.1:p.Tyr168=
ENST00000447102.7:c.504C>T ENSP00000403536.2:p.Tyr168=
ENST00000591788.2:c.189C>T ENSP00000466341.2:p.Tyr63=
NM_000156.5:c.504C>T NP_000147.1:p.Tyr168=
NM_138924.2:c.504C>T NP_620279.1:p.Tyr168=
NM_000156.6:c.504C>T MANE Select NP_000147.1:p.Tyr168=
NM_138924.3:c.504C>T NP_620279.1:p.Tyr168=