Canonical Allele Identifier: CA402995108
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399150T>C (hg19) chr19:g.1399151T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399151T>C , CM000681.2:g.1399151T>C GRCh38
NC_000019.9:g.1399150T>C , CM000681.1:g.1399150T>C GRCh37
NC_000019.8:g.1350150T>C NCBI36
NG_009785.1:g.7403A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.436A>G MANE Select ENSP00000252288.1:p.Thr146Ala
ENST00000447102.8:c.436A>G ENSP00000403536.2:p.Thr146Ala
ENST00000591788.3:c.119A>G
ENST00000640164.1:n.269A>G
ENST00000640762.1:c.367A>G ENSP00000492031.1:p.Thr123Ala
ENST00000252288.6:c.436A>G ENSP00000252288.1:p.Thr146Ala
ENST00000447102.7:c.436A>G ENSP00000403536.2:p.Thr146Ala
ENST00000591788.2:c.121A>G ENSP00000466341.2:p.Thr41Ala
NM_000156.5:c.436A>G NP_000147.1:p.Thr146Ala
NM_138924.2:c.436A>G NP_620279.1:p.Thr146Ala
NM_000156.6:c.436A>G MANE Select NP_000147.1:p.Thr146Ala
NM_138924.3:c.436A>G NP_620279.1:p.Thr146Ala
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