Canonical Allele Identifier: CA2000590767
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166855_112166856delinsAG , CM000673.2:g.112166855_112166856delinsAG GRCh38
NC_000011.9:g.112037578_112037579delinsAG , CM000673.1:g.112037578_112037579delinsAG GRCh37
NC_000011.8:g.111542788_111542789delinsAG NCBI36
NG_028143.1:g.2262_2263delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3564_320-3563delinsAG
ENST00000531744.5:c.315-3564_315-3563delinsAG ENSP00000456957.1:n.315-3564_315-3563deli...
ENST00000532699.1:c.315-3564_315-3563delinsAG ENSP00000456434.1:n.315-3564_315-3563deli...