Canonical Allele Identifier: CA2317699006
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398959T= , CM000681.2:g.1398959T= GRCh38
NC_000019.9:g.1398958T= , CM000681.1:g.1398958T= GRCh37
NC_000019.8:g.1349958T= NCBI36
NG_009785.1:g.7595A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.527A= MANE Select ENSP00000252288.1:p.Glu176=
ENST00000447102.8:c.527A= ENSP00000403536.2:p.Glu176=
ENST00000591788.3:c.210A=
ENST00000640164.1:n.360A=
ENST00000640762.1:c.458A= ENSP00000492031.1:p.Glu153=
ENST00000252288.6:c.527A= ENSP00000252288.1:p.Glu176=
ENST00000447102.7:c.527A= ENSP00000403536.2:p.Glu176=
ENST00000591788.2:c.212A= ENSP00000466341.2:p.Glu71=
NM_000156.5:c.527A= NP_000147.1:p.Glu176=
NM_138924.2:c.527A= NP_620279.1:p.Glu176=
NM_000156.6:c.527A= MANE Select NP_000147.1:p.Glu176=
NM_138924.3:c.527A= NP_620279.1:p.Glu176=