Canonical Allele Identifier: CA402994371
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1398964C>G (hg19) chr19:g.1398965C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398965C>G , CM000681.2:g.1398965C>G GRCh38
NC_000019.9:g.1398964C>G , CM000681.1:g.1398964C>G GRCh37
NC_000019.8:g.1349964C>G NCBI36
NG_009785.1:g.7589G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.521G>C MANE Select ENSP00000252288.1:p.Trp174Ser
ENST00000447102.8:c.521G>C ENSP00000403536.2:p.Trp174Ser
ENST00000591788.3:c.204G>C
ENST00000640164.1:n.354G>C
ENST00000640762.1:c.452G>C ENSP00000492031.1:p.Trp151Ser
ENST00000252288.6:c.521G>C ENSP00000252288.1:p.Trp174Ser
ENST00000447102.7:c.521G>C ENSP00000403536.2:p.Trp174Ser
ENST00000591788.2:c.206G>C ENSP00000466341.2:p.Trp69Ser
NM_000156.5:c.521G>C NP_000147.1:p.Trp174Ser
NM_138924.2:c.521G>C NP_620279.1:p.Trp174Ser
NM_000156.6:c.521G>C MANE Select NP_000147.1:p.Trp174Ser
NM_138924.3:c.521G>C NP_620279.1:p.Trp174Ser
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