Canonical Allele Identifier: CA2317699022
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398983T= , CM000681.2:g.1398983T= GRCh38
NC_000019.9:g.1398982T= , CM000681.1:g.1398982T= GRCh37
NC_000019.8:g.1349982T= NCBI36
NG_009785.1:g.7571A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.503A= MANE Select ENSP00000252288.1:p.Tyr168=
ENST00000447102.8:c.503A= ENSP00000403536.2:p.Tyr168=
ENST00000591788.3:c.186A=
ENST00000640164.1:n.336A=
ENST00000640762.1:c.434A= ENSP00000492031.1:p.Tyr145=
ENST00000252288.6:c.503A= ENSP00000252288.1:p.Tyr168=
ENST00000447102.7:c.503A= ENSP00000403536.2:p.Tyr168=
ENST00000591788.2:c.188A= ENSP00000466341.2:p.Tyr63=
NM_000156.5:c.503A= NP_000147.1:p.Tyr168=
NM_138924.2:c.503A= NP_620279.1:p.Tyr168=
NM_000156.6:c.503A= MANE Select NP_000147.1:p.Tyr168=
NM_138924.3:c.503A= NP_620279.1:p.Tyr168=