Canonical Allele Identifier: CA504895176
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399005C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399006C>A , CM000681.2:g.1399006C>A GRCh38
NC_000019.9:g.1399005C>A , CM000681.1:g.1399005C>A GRCh37
NC_000019.8:g.1350005C>A NCBI36
NG_009785.1:g.7548G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.480G>T MANE Select ENSP00000252288.1:p.Leu160=
ENST00000447102.8:c.480G>T ENSP00000403536.2:p.Leu160=
ENST00000591788.3:c.163G>T
ENST00000640164.1:n.313G>T
ENST00000640762.1:c.411G>T ENSP00000492031.1:p.Leu137=
ENST00000252288.6:c.480G>T ENSP00000252288.1:p.Leu160=
ENST00000447102.7:c.480G>T ENSP00000403536.2:p.Leu160=
ENST00000591788.2:c.165G>T ENSP00000466341.2:p.Leu55=
NM_000156.5:c.480G>T NP_000147.1:p.Leu160=
NM_138924.2:c.480G>T NP_620279.1:p.Leu160=
NM_000156.6:c.480G>T MANE Select NP_000147.1:p.Leu160=
NM_138924.3:c.480G>T NP_620279.1:p.Leu160=