Canonical Allele Identifier: CA2000590742
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166781_112166782delinsAC , CM000673.2:g.112166781_112166782delinsAC GRCh38
NC_000011.9:g.112037504_112037505delinsAC , CM000673.1:g.112037504_112037505delinsAC GRCh37
NC_000011.8:g.111542714_111542715delinsAC NCBI36
NG_028143.1:g.2336_2337delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3638_320-3637delinsAC
ENST00000531744.5:c.315-3638_315-3637delinsAC ENSP00000456957.1:n.315-3638_315-3637deli...
ENST00000532699.1:c.315-3638_315-3637delinsAC ENSP00000456434.1:n.315-3638_315-3637deli...