Canonical Allele Identifier: CA2582641142
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1399297-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399297G>T , CM000681.2:g.1399297G>T GRCh38
NC_000019.9:g.1399296G>T , CM000681.1:g.1399296G>T GRCh37
NC_000019.8:g.1350296G>T NCBI36
NG_009785.1:g.7257C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.392-102C>A MANE Select ENSP00000252288.1:n.392-102C>A
ENST00000447102.8:c.392-102C>A ENSP00000403536.2:n.392-102C>A
ENST00000591788.3:c.75-102C>A
ENST00000640164.1:n.225-102C>A
ENST00000640762.1:c.323-102C>A ENSP00000492031.1:n.323-102C>A
ENST00000252288.6:c.392-102C>A ENSP00000252288.1:n.392-102C>A
ENST00000447102.7:c.392-102C>A ENSP00000403536.2:n.392-102C>A
ENST00000591788.2:c.77-102C>A ENSP00000466341.2:n.77-102C>A
NM_000156.5:c.392-102C>A NP_000147.1:n.392-102C>A
NM_138924.2:c.392-102C>A NP_620279.1:n.392-102C>A
NM_000156.6:c.392-102C>A MANE Select NP_000147.1:n.392-102C>A
NM_138924.3:c.392-102C>A NP_620279.1:n.392-102C>A
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