Canonical Allele Identifier: CA402995155
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399156C>A , CM000681.2:g.1399156C>A GRCh38
NC_000019.9:g.1399155C>A , CM000681.1:g.1399155C>A GRCh37
NC_000019.8:g.1350155C>A NCBI36
NG_009785.1:g.7398G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.431G>T MANE Select ENSP00000252288.1:p.Trp144Leu
ENST00000447102.8:c.431G>T ENSP00000403536.2:p.Trp144Leu
ENST00000591788.3:c.114G>T
ENST00000640164.1:n.264G>T
ENST00000640762.1:c.362G>T ENSP00000492031.1:p.Trp121Leu
ENST00000252288.6:c.431G>T ENSP00000252288.1:p.Trp144Leu
ENST00000447102.7:c.431G>T ENSP00000403536.2:p.Trp144Leu
ENST00000591788.2:c.116G>T ENSP00000466341.2:p.Trp39Leu
NM_000156.5:c.431G>T NP_000147.1:p.Trp144Leu
NM_138924.2:c.431G>T NP_620279.1:p.Trp144Leu
NM_000156.6:c.431G>T MANE Select NP_000147.1:p.Trp144Leu
NM_138924.3:c.431G>T NP_620279.1:p.Trp144Leu