Canonical Allele Identifier: CA9043647
Gene: GAMT HGNC NCBI

Linked Data

dbSNP Id: rs374874882
ExAC: 19:1399088 C / T
gnomAD v2: 19-1399088-C-T
gnomAD v3: 19-1399089-C-T
gnomAD v4: 19-1399089-C-T
MyVariant Identifiers: chr19:g.1399088C>T (hg19) chr19:g.1399089C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399089C>T , CM000681.2:g.1399089C>T GRCh38
NC_000019.9:g.1399088C>T , CM000681.1:g.1399088C>T GRCh37
NC_000019.8:g.1350088C>T NCBI36
NG_009785.1:g.7465G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.459+39G>A MANE Select ENSP00000252288.1:n.459+39G>A
ENST00000447102.8:c.459+39G>A ENSP00000403536.2:n.459+39G>A
ENST00000591788.3:c.142+39G>A
ENST00000640164.1:n.292+39G>A
ENST00000640762.1:c.390+39G>A ENSP00000492031.1:n.390+39G>A
ENST00000252288.6:c.459+39G>A ENSP00000252288.1:n.459+39G>A
ENST00000447102.7:c.459+39G>A ENSP00000403536.2:n.459+39G>A
ENST00000591788.2:c.144+39G>A ENSP00000466341.2:n.144+39G>A
NM_000156.5:c.459+39G>A NP_000147.1:n.459+39G>A
NM_138924.2:c.459+39G>A NP_620279.1:n.459+39G>A
NM_000156.6:c.459+39G>A MANE Select NP_000147.1:n.459+39G>A
NM_138924.3:c.459+39G>A NP_620279.1:n.459+39G>A
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