Canonical Allele Identifier: CA2317699047
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399023G= , CM000681.2:g.1399023G= GRCh38
NC_000019.9:g.1399022G= , CM000681.1:g.1399022G= GRCh37
NC_000019.8:g.1350022G= NCBI36
NG_009785.1:g.7531C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.463C= MANE Select ENSP00000252288.1:p.His155=
ENST00000447102.8:c.463C= ENSP00000403536.2:p.His155=
ENST00000591788.3:c.146C=
ENST00000640164.1:n.296C=
ENST00000640762.1:c.394C= ENSP00000492031.1:p.His132=
ENST00000252288.6:c.463C= ENSP00000252288.1:p.His155=
ENST00000447102.7:c.463C= ENSP00000403536.2:p.His155=
ENST00000591788.2:c.148C= ENSP00000466341.2:p.His50=
NM_000156.5:c.463C= NP_000147.1:p.His155=
NM_138924.2:c.463C= NP_620279.1:p.His155=
NM_000156.6:c.463C= MANE Select NP_000147.1:p.His155=
NM_138924.3:c.463C= NP_620279.1:p.His155=