Canonical Allele Identifier: CA504730060
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399130G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399131G>A , CM000681.2:g.1399131G>A GRCh38
NC_000019.9:g.1399130G>A , CM000681.1:g.1399130G>A GRCh37
NC_000019.8:g.1350130G>A NCBI36
NG_009785.1:g.7423C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.456C>T MANE Select ENSP00000252288.1:p.Ile152=
ENST00000447102.8:c.456C>T ENSP00000403536.2:p.Ile152=
ENST00000591788.3:c.139C>T
ENST00000640164.1:n.289C>T
ENST00000640762.1:c.387C>T ENSP00000492031.1:p.Ile129=
ENST00000252288.6:c.456C>T ENSP00000252288.1:p.Ile152=
ENST00000447102.7:c.456C>T ENSP00000403536.2:p.Ile152=
ENST00000591788.2:c.141C>T ENSP00000466341.2:p.Ile47=
NM_000156.5:c.456C>T NP_000147.1:p.Ile152=
NM_138924.2:c.456C>T NP_620279.1:p.Ile152=
NM_000156.6:c.456C>T MANE Select NP_000147.1:p.Ile152=
NM_138924.3:c.456C>T NP_620279.1:p.Ile152=