Canonical Allele Identifier: CA2582641098
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1399121-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399121G>A , CM000681.2:g.1399121G>A GRCh38
NC_000019.9:g.1399120G>A , CM000681.1:g.1399120G>A GRCh37
NC_000019.8:g.1350120G>A NCBI36
NG_009785.1:g.7433C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.459+7C>T MANE Select ENSP00000252288.1:n.459+7C>T
ENST00000447102.8:c.459+7C>T ENSP00000403536.2:n.459+7C>T
ENST00000591788.3:c.142+7C>T
ENST00000640164.1:n.292+7C>T
ENST00000640762.1:c.390+7C>T ENSP00000492031.1:n.390+7C>T
ENST00000252288.6:c.459+7C>T ENSP00000252288.1:n.459+7C>T
ENST00000447102.7:c.459+7C>T ENSP00000403536.2:n.459+7C>T
ENST00000591788.2:c.144+7C>T ENSP00000466341.2:n.144+7C>T
NM_000156.5:c.459+7C>T NP_000147.1:n.459+7C>T
NM_138924.2:c.459+7C>T NP_620279.1:n.459+7C>T
NM_000156.6:c.459+7C>T MANE Select NP_000147.1:n.459+7C>T
NM_138924.3:c.459+7C>T NP_620279.1:n.459+7C>T
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