Canonical Allele Identifier: CA9043637

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399019G>T , CM000681.2:g.1399019G>T	GRCh38
NC_000019.9:g.1399018G>T , CM000681.1:g.1399018G>T	GRCh37
NC_000019.8:g.1350018G>T	NCBI36
NG_009785.1:g.7535C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000156.6:c.467C>A MANE Select	NP_000147.1:p.Ala156Asp
ENST00000252288.8:c.467C>A MANE Select	ENSP00000252288.1:p.Ala156Asp
NM_000156.5:c.467C>A	NP_000147.1:p.Ala156Asp
NM_138924.2:c.467C>A	NP_620279.1:p.Ala156Asp
NM_138924.3:c.467C>A	NP_620279.1:p.Ala156Asp
ENST00000252288.6:c.467C>A	ENSP00000252288.1:p.Ala156Asp
ENST00000447102.7:c.467C>A	ENSP00000403536.2:p.Ala156Asp
ENST00000447102.8:c.467C>A	ENSP00000403536.2:p.Ala156Asp
ENST00000591788.2:c.152C>A	ENSP00000466341.2:p.Ala51Asp
ENST00000591788.3:c.150C>A
ENST00000640164.1:n.300C>A
ENST00000640762.1:c.398C>A	ENSP00000492031.1:p.Ala133Asp