Canonical Allele Identifier: CA2582641832
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1401252-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401252T>G , CM000681.2:g.1401252T>G GRCh38
NC_000019.9:g.1401251T>G , CM000681.1:g.1401251T>G GRCh37
NC_000019.8:g.1352251T>G NCBI36
NG_009785.1:g.5302A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.181+44A>C MANE Select ENSP00000252288.1:n.181+44A>C
ENST00000447102.8:c.181+44A>C ENSP00000403536.2:n.181+44A>C
ENST00000640762.1:c.112+113A>C ENSP00000492031.1:n.112+113A>C
ENST00000252288.6:c.181+44A>C ENSP00000252288.1:n.181+44A>C
ENST00000447102.7:c.181+44A>C ENSP00000403536.2:n.181+44A>C
NM_000156.5:c.181+44A>C NP_000147.1:n.181+44A>C
NM_138924.2:c.181+44A>C NP_620279.1:n.181+44A>C
NM_000156.6:c.181+44A>C MANE Select NP_000147.1:n.181+44A>C
NM_138924.3:c.181+44A>C NP_620279.1:n.181+44A>C
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