Canonical Allele Identifier: CA2582641732
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1401170-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401170A>G , CM000681.2:g.1401170A>G GRCh38
NC_000019.9:g.1401169A>G , CM000681.1:g.1401169A>G GRCh37
NC_000019.8:g.1352169A>G NCBI36
NG_009785.1:g.5384T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+126T>C MANE Select ENSP00000252288.1:n.181+126T>C
ENST00000447102.8:c.181+126T>C ENSP00000403536.2:n.181+126T>C
ENST00000640762.1:c.112+195T>C ENSP00000492031.1:n.112+195T>C
ENST00000252288.6:c.181+126T>C ENSP00000252288.1:n.181+126T>C
ENST00000447102.7:c.181+126T>C ENSP00000403536.2:n.181+126T>C
NM_000156.5:c.181+126T>C NP_000147.1:n.181+126T>C
NM_138924.2:c.181+126T>C NP_620279.1:n.181+126T>C
NM_000156.6:c.181+126T>C MANE Select NP_000147.1:n.181+126T>C
NM_138924.3:c.181+126T>C NP_620279.1:n.181+126T>C
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