Canonical Allele Identifier: CA2317699109
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399134_1399135delinsGA , CM000681.2:g.1399134_1399135delinsGA GRCh38
NC_000019.9:g.1399133_1399134delinsGA , CM000681.1:g.1399133_1399134delinsGA GRCh37
NC_000019.8:g.1350133_1350134delinsGA NCBI36
NG_009785.1:g.7419_7420delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.452_453delinsTC MANE Select ENSP00000252288.1:p.Phe151=
ENST00000447102.8:c.452_453delinsTC ENSP00000403536.2:p.Phe151=
ENST00000591788.3:c.135_136delinsTC
ENST00000640164.1:n.285_286delinsTC
ENST00000640762.1:c.383_384delinsTC ENSP00000492031.1:p.Phe128=
ENST00000252288.6:c.452_453delinsTC ENSP00000252288.1:p.Phe151=
ENST00000447102.7:c.452_453delinsTC ENSP00000403536.2:p.Phe151=
ENST00000591788.2:c.137_138delinsTC ENSP00000466341.2:p.Phe46=
NM_000156.5:c.452_453delinsTC NP_000147.1:p.Phe151=
NM_138924.2:c.452_453delinsTC NP_620279.1:p.Phe151=
NM_000156.6:c.452_453delinsTC MANE Select NP_000147.1:p.Phe151=
NM_138924.3:c.452_453delinsTC NP_620279.1:p.Phe151=