Canonical Allele Identifier: CA504895146
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1398988-G-C
MyVariant Identifiers: chr19:g.1398987G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398988G>C , CM000681.2:g.1398988G>C GRCh38
NC_000019.9:g.1398987G>C , CM000681.1:g.1398987G>C GRCh37
NC_000019.8:g.1349987G>C NCBI36
NG_009785.1:g.7566C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.498C>G MANE Select ENSP00000252288.1:p.Leu166=
ENST00000447102.8:c.498C>G ENSP00000403536.2:p.Leu166=
ENST00000591788.3:c.181C>G
ENST00000640164.1:n.331C>G
ENST00000640762.1:c.429C>G ENSP00000492031.1:p.Leu143=
ENST00000252288.6:c.498C>G ENSP00000252288.1:p.Leu166=
ENST00000447102.7:c.498C>G ENSP00000403536.2:p.Leu166=
ENST00000591788.2:c.183C>G ENSP00000466341.2:p.Leu61=
NM_000156.5:c.498C>G NP_000147.1:p.Leu166=
NM_138924.2:c.498C>G NP_620279.1:p.Leu166=
NM_000156.6:c.498C>G MANE Select NP_000147.1:p.Leu166=
NM_138924.3:c.498C>G NP_620279.1:p.Leu166=