Canonical Allele Identifier: CA504730136
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1399191-G-A
MyVariant Identifiers: chr19:g.1399190G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399191G>A , CM000681.2:g.1399191G>A GRCh38
NC_000019.9:g.1399190G>A , CM000681.1:g.1399190G>A GRCh37
NC_000019.8:g.1350190G>A NCBI36
NG_009785.1:g.7363C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.396C>T MANE Select ENSP00000252288.1:p.Ile132=
ENST00000447102.8:c.396C>T ENSP00000403536.2:p.Ile132=
ENST00000591788.3:c.79C>T
ENST00000640164.1:n.229C>T
ENST00000640762.1:c.327C>T ENSP00000492031.1:p.Ile109=
ENST00000252288.6:c.396C>T ENSP00000252288.1:p.Ile132=
ENST00000447102.7:c.396C>T ENSP00000403536.2:p.Ile132=
ENST00000591788.2:c.81C>T ENSP00000466341.2:p.Ile27=
NM_000156.5:c.396C>T NP_000147.1:p.Ile132=
NM_138924.2:c.396C>T NP_620279.1:p.Ile132=
NM_000156.6:c.396C>T MANE Select NP_000147.1:p.Ile132=
NM_138924.3:c.396C>T NP_620279.1:p.Ile132=