Canonical Allele Identifier: CA504731765
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2035678
ClinVar RCV Id: RCV002877579
gnomAD v4: 19-1401471-G-A
MyVariant Identifiers: chr19:g.1401470G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401471G>A , CM000681.2:g.1401471G>A GRCh38
NC_000019.9:g.1401470G>A , CM000681.1:g.1401470G>A GRCh37
NC_000019.8:g.1352470G>A NCBI36
NG_009785.1:g.5083C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.6C>T MANE Select ENSP00000252288.1:p.Ser2=
ENST00000447102.8:c.6C>T ENSP00000403536.2:p.Ser2=
ENST00000640762.1:c.6C>T ENSP00000492031.1:p.Ser2=
ENST00000252288.6:c.6C>T ENSP00000252288.1:p.Ser2=
ENST00000447102.7:c.6C>T ENSP00000403536.2:p.Ser2=
NM_000156.5:c.6C>T NP_000147.1:p.Ser2=
NM_138924.2:c.6C>T NP_620279.1:p.Ser2=
NM_000156.6:c.6C>T MANE Select NP_000147.1:p.Ser2=
NM_138924.3:c.6C>T NP_620279.1:p.Ser2=