Canonical Allele Identifier: CA504895202
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399017G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399018G>A , CM000681.2:g.1399018G>A GRCh38
NC_000019.9:g.1399017G>A , CM000681.1:g.1399017G>A GRCh37
NC_000019.8:g.1350017G>A NCBI36
NG_009785.1:g.7536C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.468C>T MANE Select ENSP00000252288.1:p.Ala156=
ENST00000447102.8:c.468C>T ENSP00000403536.2:p.Ala156=
ENST00000591788.3:c.151C>T
ENST00000640164.1:n.301C>T
ENST00000640762.1:c.399C>T ENSP00000492031.1:p.Ala133=
ENST00000252288.6:c.468C>T ENSP00000252288.1:p.Ala156=
ENST00000447102.7:c.468C>T ENSP00000403536.2:p.Ala156=
ENST00000591788.2:c.153C>T ENSP00000466341.2:p.Ala51=
NM_000156.5:c.468C>T NP_000147.1:p.Ala156=
NM_138924.2:c.468C>T NP_620279.1:p.Ala156=
NM_000156.6:c.468C>T MANE Select NP_000147.1:p.Ala156=
NM_138924.3:c.468C>T NP_620279.1:p.Ala156=