Canonical Allele Identifier: CA1694872883
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282658_24282659delinsCT , CM000669.2:g.24282658_24282659delinsCT GRCh38
NC_000007.13:g.24322277_24322278delinsCT , CM000669.1:g.24322277_24322278delinsCT GRCh37
NC_000007.12:g.24288802_24288803delinsCT NCBI36
NG_016148.1:g.3471_3472delinsCT

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-26960_42-26959delinsAG XP_016868399.1:n.42-26960_42-26959delinsAG
XM_017012911.1:c.42-26960_42-26959delinsAG XP_016868400.1:n.42-26960_42-26959delinsAG
XR_001745121.1:n.473+36698_473+36699delinsAG
XR_001745122.1:n.345-85630_345-85629delinsAG
XR_001745123.1:n.473+36698_473+36699delinsAG
XR_001745124.1:n.473+36698_473+36699delinsAG
XR_001745125.1:n.473+36698_473+36699delinsAG
XR_001745126.1:n.473+36698_473+36699delinsAG
XR_001745127.1:n.345-26960_345-26959delinsAG
XR_001745129.1:n.473+36698_473+36699delinsAG
XR_001745130.1:n.473+36698_473+36699delinsAG
XR_001745131.1:n.473+36698_473+36699delinsAG
XR_001745132.1:n.473+36698_473+36699delinsAG