Canonical Allele Identifier: CA2317698967
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398867A= , CM000681.2:g.1398867A= GRCh38
NC_000019.9:g.1398866A= , CM000681.1:g.1398866A= GRCh37
NC_000019.8:g.1349866A= NCBI36
NG_009785.1:g.7687T=

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.570+49T= MANE Select ENSP00000252288.1:n.570+49T=
ENST00000447102.8:c.619T= ENSP00000403536.2:p.Trp207=
ENST00000591788.3:c.253+49T=
ENST00000640164.1:n.403+49T=
ENST00000640762.1:c.501+49T= ENSP00000492031.1:n.501+49T=
ENST00000252288.6:c.570+49T= ENSP00000252288.1:n.570+49T=
ENST00000447102.7:c.619T= ENSP00000403536.2:p.Trp207=
ENST00000591788.2:c.255+49T= ENSP00000466341.2:n.255+49T=
NM_000156.5:c.570+49T= NP_000147.1:n.570+49T=
NM_138924.2:c.619T= NP_620279.1:p.Trp207=
NM_000156.6:c.570+49T= MANE Select NP_000147.1:n.570+49T=
NM_138924.3:c.619T= NP_620279.1:p.Trp207=