Canonical Allele Identifier: CA402995042
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1399144-T-G
MyVariant Identifiers: chr19:g.1399143T>G (hg19) chr19:g.1399144T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399144T>G , CM000681.2:g.1399144T>G GRCh38
NC_000019.9:g.1399143T>G , CM000681.1:g.1399143T>G GRCh37
NC_000019.8:g.1350143T>G NCBI36
NG_009785.1:g.7410A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.443A>C MANE Select ENSP00000252288.1:p.Gln148Pro
ENST00000447102.8:c.443A>C ENSP00000403536.2:p.Gln148Pro
ENST00000591788.3:c.126A>C
ENST00000640164.1:n.276A>C
ENST00000640762.1:c.374A>C ENSP00000492031.1:p.Gln125Pro
ENST00000252288.6:c.443A>C ENSP00000252288.1:p.Gln148Pro
ENST00000447102.7:c.443A>C ENSP00000403536.2:p.Gln148Pro
ENST00000591788.2:c.128A>C ENSP00000466341.2:p.Gln43Pro
NM_000156.5:c.443A>C NP_000147.1:p.Gln148Pro
NM_138924.2:c.443A>C NP_620279.1:p.Gln148Pro
NM_000156.6:c.443A>C MANE Select NP_000147.1:p.Gln148Pro
NM_138924.3:c.443A>C NP_620279.1:p.Gln148Pro
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