Canonical Allele Identifier: CA402994939
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399132T>A (hg19) chr19:g.1399133T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399133T>A , CM000681.2:g.1399133T>A GRCh38
NC_000019.9:g.1399132T>A , CM000681.1:g.1399132T>A GRCh37
NC_000019.8:g.1350132T>A NCBI36
NG_009785.1:g.7421A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.454A>T MANE Select ENSP00000252288.1:p.Ile152Phe
ENST00000447102.8:c.454A>T ENSP00000403536.2:p.Ile152Phe
ENST00000591788.3:c.137A>T
ENST00000640164.1:n.287A>T
ENST00000640762.1:c.385A>T ENSP00000492031.1:p.Ile129Phe
ENST00000252288.6:c.454A>T ENSP00000252288.1:p.Ile152Phe
ENST00000447102.7:c.454A>T ENSP00000403536.2:p.Ile152Phe
ENST00000591788.2:c.139A>T ENSP00000466341.2:p.Ile47Phe
NM_000156.5:c.454A>T NP_000147.1:p.Ile152Phe
NM_138924.2:c.454A>T NP_620279.1:p.Ile152Phe
NM_000156.6:c.454A>T MANE Select NP_000147.1:p.Ile152Phe
NM_138924.3:c.454A>T NP_620279.1:p.Ile152Phe
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