Canonical Allele Identifier: CA2576548763
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1401222-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401226del , CM000681.2:g.1401226del GRCh38
NC_000019.9:g.1401225del , CM000681.1:g.1401225del GRCh37
NC_000019.8:g.1352225del NCBI36
NG_009785.1:g.5331del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+73del MANE Select ENSP00000252288.1:n.181+73del
ENST00000447102.8:c.181+73del ENSP00000403536.2:n.181+73del
ENST00000640762.1:c.112+142del ENSP00000492031.1:n.112+142del
ENST00000252288.6:c.181+73del ENSP00000252288.1:n.181+73del
ENST00000447102.7:c.181+73del ENSP00000403536.2:n.181+73del
NM_000156.5:c.181+73del NP_000147.1:n.181+73del
NM_138924.2:c.181+73del NP_620279.1:n.181+73del
NM_000156.6:c.181+73del MANE Select NP_000147.1:n.181+73del
NM_138924.3:c.181+73del NP_620279.1:n.181+73del
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