Canonical Allele Identifier: CA2317698966
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398866C= , CM000681.2:g.1398866C= GRCh38
NC_000019.9:g.1398865C= , CM000681.1:g.1398865C= GRCh37
NC_000019.8:g.1349865C= NCBI36
NG_009785.1:g.7688G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.570+50G= MANE Select ENSP00000252288.1:n.570+50G=
ENST00000447102.8:c.620G= ENSP00000403536.2:p.Trp207=
ENST00000591788.3:c.253+50G=
ENST00000640164.1:n.403+50G=
ENST00000640762.1:c.501+50G= ENSP00000492031.1:n.501+50G=
ENST00000252288.6:c.570+50G= ENSP00000252288.1:n.570+50G=
ENST00000447102.7:c.620G= ENSP00000403536.2:p.Trp207=
ENST00000591788.2:c.255+50G= ENSP00000466341.2:n.255+50G=
NM_000156.5:c.570+50G= NP_000147.1:n.570+50G=
NM_138924.2:c.620G= NP_620279.1:p.Trp207=
NM_000156.6:c.570+50G= MANE Select NP_000147.1:n.570+50G=
NM_138924.3:c.620G= NP_620279.1:p.Trp207=