Canonical Allele Identifier: CA402995034
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399141A>G (hg19) chr19:g.1399142A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399142A>G , CM000681.2:g.1399142A>G GRCh38
NC_000019.9:g.1399141A>G , CM000681.1:g.1399141A>G GRCh37
NC_000019.8:g.1350141A>G NCBI36
NG_009785.1:g.7412T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.445T>C MANE Select ENSP00000252288.1:p.Phe149Leu
ENST00000447102.8:c.445T>C ENSP00000403536.2:p.Phe149Leu
ENST00000591788.3:c.128T>C
ENST00000640164.1:n.278T>C
ENST00000640762.1:c.376T>C ENSP00000492031.1:p.Phe126Leu
ENST00000252288.6:c.445T>C ENSP00000252288.1:p.Phe149Leu
ENST00000447102.7:c.445T>C ENSP00000403536.2:p.Phe149Leu
ENST00000591788.2:c.130T>C ENSP00000466341.2:p.Phe44Leu
NM_000156.5:c.445T>C NP_000147.1:p.Phe149Leu
NM_138924.2:c.445T>C NP_620279.1:p.Phe149Leu
NM_000156.6:c.445T>C MANE Select NP_000147.1:p.Phe149Leu
NM_138924.3:c.445T>C NP_620279.1:p.Phe149Leu
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