Canonical Allele Identifier: CA402994536
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1398981G>T (hg19) chr19:g.1398982G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.504C>A MANE Select ENSP00000252288.1:p.Tyr168Ter
ENST00000447102.8:c.504C>A ENSP00000403536.2:p.Tyr168Ter
ENST00000591788.3:c.187C>A
ENST00000640164.1:n.337C>A
ENST00000640762.1:c.435C>A ENSP00000492031.1:p.Tyr145Ter
ENST00000252288.6:c.504C>A ENSP00000252288.1:p.Tyr168Ter
ENST00000447102.7:c.504C>A ENSP00000403536.2:p.Tyr168Ter
ENST00000591788.2:c.189C>A ENSP00000466341.2:p.Tyr63Ter
NM_000156.5:c.504C>A NP_000147.1:p.Tyr168Ter
NM_138924.2:c.504C>A NP_620279.1:p.Tyr168Ter
NM_000156.6:c.504C>A MANE Select NP_000147.1:p.Tyr168Ter
NM_138924.3:c.504C>A NP_620279.1:p.Tyr168Ter
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