Canonical Allele Identifier: CA2317699040
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399015A= , CM000681.2:g.1399015A= GRCh38
NC_000019.9:g.1399014A= , CM000681.1:g.1399014A= GRCh37
NC_000019.8:g.1350014A= NCBI36
NG_009785.1:g.7539T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.471T= MANE Select ENSP00000252288.1:p.Phe157=
ENST00000447102.8:c.471T= ENSP00000403536.2:p.Phe157=
ENST00000591788.3:c.154T=
ENST00000640164.1:n.304T=
ENST00000640762.1:c.402T= ENSP00000492031.1:p.Phe134=
ENST00000252288.6:c.471T= ENSP00000252288.1:p.Phe157=
ENST00000447102.7:c.471T= ENSP00000403536.2:p.Phe157=
ENST00000591788.2:c.156T= ENSP00000466341.2:p.Phe52=
NM_000156.5:c.471T= NP_000147.1:p.Phe157=
NM_138924.2:c.471T= NP_620279.1:p.Phe157=
NM_000156.6:c.471T= MANE Select NP_000147.1:p.Phe157=
NM_138924.3:c.471T= NP_620279.1:p.Phe157=