Canonical Allele Identifier: CA2317699165
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399231G= , CM000681.2:g.1399231G= GRCh38
NC_000019.9:g.1399230G= , CM000681.1:g.1399230G= GRCh37
NC_000019.8:g.1350230G= NCBI36
NG_009785.1:g.7323C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.392-36C= MANE Select ENSP00000252288.1:n.392-36C=
ENST00000447102.8:c.392-36C= ENSP00000403536.2:n.392-36C=
ENST00000591788.3:c.75-36C=
ENST00000640164.1:n.225-36C=
ENST00000640762.1:c.323-36C= ENSP00000492031.1:n.323-36C=
ENST00000252288.6:c.392-36C= ENSP00000252288.1:n.392-36C=
ENST00000447102.7:c.392-36C= ENSP00000403536.2:n.392-36C=
ENST00000591788.2:c.77-36C= ENSP00000466341.2:n.77-36C=
NM_000156.5:c.392-36C= NP_000147.1:n.392-36C=
NM_138924.2:c.392-36C= NP_620279.1:n.392-36C=
NM_000156.6:c.392-36C= MANE Select NP_000147.1:n.392-36C=
NM_138924.3:c.392-36C= NP_620279.1:n.392-36C=