Canonical Allele Identifier: CA2582641930
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401469del , CM000681.2:g.1401469del GRCh38
NC_000019.9:g.1401468del , CM000681.1:g.1401468del GRCh37
NC_000019.8:g.1352468del NCBI36
NG_009785.1:g.5089del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.12del MANE Select ENSP00000252288.1:p.Ser5AlafsTer?
ENST00000447102.8:c.12del ENSP00000403536.2:p.Ser5AlafsTer?
ENST00000640762.1:c.12del ENSP00000492031.1:p.Ser5AlafsTer?
ENST00000252288.6:c.12del ENSP00000252288.1:p.Ser5AlafsTer?
ENST00000447102.7:c.12del ENSP00000403536.2:p.Ser5AlafsTer?
NM_000156.5:c.12del NP_000147.1:p.Ser5AlafsTer?
NM_138924.2:c.12del NP_620279.1:p.Ser5AlafsTer?
NM_000156.6:c.12del MANE Select NP_000147.1:p.Ser5AlafsTer?
NM_138924.3:c.12del NP_620279.1:p.Ser5AlafsTer?