Canonical Allele Identifier: CA504731628
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1401348-C-T
MyVariant Identifiers: chr19:g.1401347C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401348C>T , CM000681.2:g.1401348C>T GRCh38
NC_000019.9:g.1401347C>T , CM000681.1:g.1401347C>T GRCh37
NC_000019.8:g.1352347C>T NCBI36
NG_009785.1:g.5206G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.129G>A MANE Select ENSP00000252288.1:p.Glu43=
ENST00000447102.8:c.129G>A ENSP00000403536.2:p.Glu43=
ENST00000640762.1:c.112+17G>A ENSP00000492031.1:n.112+17G>A
ENST00000252288.6:c.129G>A ENSP00000252288.1:p.Glu43=
ENST00000447102.7:c.129G>A ENSP00000403536.2:p.Glu43=
NM_000156.5:c.129G>A NP_000147.1:p.Glu43=
NM_138924.2:c.129G>A NP_620279.1:p.Glu43=
NM_000156.6:c.129G>A MANE Select NP_000147.1:p.Glu43=
NM_138924.3:c.129G>A NP_620279.1:p.Glu43=