Canonical Allele Identifier: CA2000590749
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166793_112166794delinsAC , CM000673.2:g.112166793_112166794delinsAC GRCh38
NC_000011.9:g.112037516_112037517delinsAC , CM000673.1:g.112037516_112037517delinsAC GRCh37
NC_000011.8:g.111542726_111542727delinsAC NCBI36
NG_028143.1:g.2324_2325delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3626_320-3625delinsAC
ENST00000531744.5:c.315-3626_315-3625delinsAC ENSP00000456957.1:n.315-3626_315-3625deli...
ENST00000532699.1:c.315-3626_315-3625delinsAC ENSP00000456434.1:n.315-3626_315-3625deli...