Canonical Allele Identifier: CA1694873373
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283655_24283656delinsGT , CM000669.2:g.24283655_24283656delinsGT GRCh38
NC_000007.13:g.24323274_24323275delinsGT , CM000669.1:g.24323274_24323275delinsGT GRCh37
NC_000007.12:g.24289799_24289800delinsGT NCBI36
NG_016148.1:g.4468_4469delinsGT

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-27957_42-27956delinsAC XP_016868399.1:n.42-27957_42-27956delinsA...
XM_017012911.1:c.42-27957_42-27956delinsAC XP_016868400.1:n.42-27957_42-27956delinsA...
XR_001745121.1:n.473+35701_473+35702delinsAC
XR_001745122.1:n.345-86627_345-86626delinsAC
XR_001745123.1:n.473+35701_473+35702delinsAC
XR_001745124.1:n.473+35701_473+35702delinsAC
XR_001745125.1:n.473+35701_473+35702delinsAC
XR_001745126.1:n.473+35701_473+35702delinsAC
XR_001745127.1:n.345-27957_345-27956delinsAC
XR_001745129.1:n.473+35701_473+35702delinsAC
XR_001745130.1:n.473+35701_473+35702delinsAC
XR_001745131.1:n.473+35701_473+35702delinsAC
XR_001745132.1:n.473+35701_473+35702delinsAC