Canonical Allele Identifier: CA402994981
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399138T>A , CM000681.2:g.1399138T>A GRCh38
NC_000019.9:g.1399137T>A , CM000681.1:g.1399137T>A GRCh37
NC_000019.8:g.1350137T>A NCBI36
NG_009785.1:g.7416A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.449A>T MANE Select ENSP00000252288.1:p.Asn150Ile
ENST00000447102.8:c.449A>T ENSP00000403536.2:p.Asn150Ile
ENST00000591788.3:c.132A>T
ENST00000640164.1:n.282A>T
ENST00000640762.1:c.380A>T ENSP00000492031.1:p.Asn127Ile
ENST00000252288.6:c.449A>T ENSP00000252288.1:p.Asn150Ile
ENST00000447102.7:c.449A>T ENSP00000403536.2:p.Asn150Ile
ENST00000591788.2:c.134A>T ENSP00000466341.2:p.Asn45Ile
NM_000156.5:c.449A>T NP_000147.1:p.Asn150Ile
NM_138924.2:c.449A>T NP_620279.1:p.Asn150Ile
NM_000156.6:c.449A>T MANE Select NP_000147.1:p.Asn150Ile
NM_138924.3:c.449A>T NP_620279.1:p.Asn150Ile