Canonical Allele Identifier: CA1694873508
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283874_24283878delinsGGAAA , CM000669.2:g.24283874_24283878delinsGGAAA GRCh38
NC_000007.13:g.24323493_24323497delinsGGAAA , CM000669.1:g.24323493_24323497delinsGGAAA GRCh37
NC_000007.12:g.24290018_24290022delinsGGAAA NCBI36
NG_016148.1:g.4687_4691delinsGGAAA

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-28179_42-28175delinsTTTCC XP_016868399.1:n.42-28179_42-28175delinsT...
XM_017012911.1:c.42-28179_42-28175delinsTTTCC XP_016868400.1:n.42-28179_42-28175delinsT...
XR_001745121.1:n.473+35479_473+35483delinsTTTCC
XR_001745122.1:n.345-86849_345-86845delinsTTTCC
XR_001745123.1:n.473+35479_473+35483delinsTTTCC
XR_001745124.1:n.473+35479_473+35483delinsTTTCC
XR_001745125.1:n.473+35479_473+35483delinsTTTCC
XR_001745126.1:n.473+35479_473+35483delinsTTTCC
XR_001745127.1:n.345-28179_345-28175delinsTTTCC
XR_001745129.1:n.473+35479_473+35483delinsTTTCC
XR_001745130.1:n.473+35479_473+35483delinsTTTCC
XR_001745131.1:n.473+35479_473+35483delinsTTTCC
XR_001745132.1:n.473+35479_473+35483delinsTTTCC