Canonical Allele Identifier: CA402995906

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399587C>T , CM000681.2:g.1399587C>T	GRCh38
NC_000019.9:g.1399586C>T , CM000681.1:g.1399586C>T	GRCh37
NC_000019.8:g.1350586C>T	NCBI36
NG_009785.1:g.6967G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.328G>A MANE Select	ENSP00000252288.1:p.Val110Ile
ENST00000447102.8:c.328G>A	ENSP00000403536.2:p.Val110Ile
ENST00000591788.3:c.11G>A
ENST00000640164.1:n.161G>A
ENST00000640762.1:c.259G>A	ENSP00000492031.1:p.Val87Ile
ENST00000252288.6:c.328G>A	ENSP00000252288.1:p.Val110Ile
ENST00000447102.7:c.328G>A	ENSP00000403536.2:p.Val110Ile
ENST00000591788.2:c.13G>A	ENSP00000466341.2:p.Val5Ile
NM_000156.5:c.328G>A	NP_000147.1:p.Val110Ile
NM_138924.2:c.328G>A	NP_620279.1:p.Val110Ile
NM_000156.6:c.328G>A MANE Select	NP_000147.1:p.Val110Ile
NM_138924.3:c.328G>A	NP_620279.1:p.Val110Ile