Canonical Allele Identifier: CA2317699139
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399180G= , CM000681.2:g.1399180G= GRCh38
NC_000019.9:g.1399179G= , CM000681.1:g.1399179G= GRCh37
NC_000019.8:g.1350179G= NCBI36
NG_009785.1:g.7374C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.407C= MANE Select ENSP00000252288.1:p.Thr136=
ENST00000447102.8:c.407C= ENSP00000403536.2:p.Thr136=
ENST00000591788.3:c.90C=
ENST00000640164.1:n.240C=
ENST00000640762.1:c.338C= ENSP00000492031.1:p.Thr113=
ENST00000252288.6:c.407C= ENSP00000252288.1:p.Thr136=
ENST00000447102.7:c.407C= ENSP00000403536.2:p.Thr136=
ENST00000591788.2:c.92C= ENSP00000466341.2:p.Thr31=
NM_000156.5:c.407C= NP_000147.1:p.Thr136=
NM_138924.2:c.407C= NP_620279.1:p.Thr136=
NM_000156.6:c.407C= MANE Select NP_000147.1:p.Thr136=
NM_138924.3:c.407C= NP_620279.1:p.Thr136=