Canonical Allele Identifier: CA402994957
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399134A>T (hg19) chr19:g.1399135A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399135A>T , CM000681.2:g.1399135A>T GRCh38
NC_000019.9:g.1399134A>T , CM000681.1:g.1399134A>T GRCh37
NC_000019.8:g.1350134A>T NCBI36
NG_009785.1:g.7419T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.452T>A MANE Select ENSP00000252288.1:p.Phe151Tyr
ENST00000447102.8:c.452T>A ENSP00000403536.2:p.Phe151Tyr
ENST00000591788.3:c.135T>A
ENST00000640164.1:n.285T>A
ENST00000640762.1:c.383T>A ENSP00000492031.1:p.Phe128Tyr
ENST00000252288.6:c.452T>A ENSP00000252288.1:p.Phe151Tyr
ENST00000447102.7:c.452T>A ENSP00000403536.2:p.Phe151Tyr
ENST00000591788.2:c.137T>A ENSP00000466341.2:p.Phe46Tyr
NM_000156.5:c.452T>A NP_000147.1:p.Phe151Tyr
NM_138924.2:c.452T>A NP_620279.1:p.Phe151Tyr
NM_000156.6:c.452T>A MANE Select NP_000147.1:p.Phe151Tyr
NM_138924.3:c.452T>A NP_620279.1:p.Phe151Tyr
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