Canonical Allele Identifier: CA1694873216
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283403_24283405delinsGCT , CM000669.2:g.24283403_24283405delinsGCT GRCh38
NC_000007.13:g.24323022_24323024delinsGCT , CM000669.1:g.24323022_24323024delinsGCT GRCh37
NC_000007.12:g.24289547_24289549delinsGCT NCBI36
NG_016148.1:g.4216_4218delinsGCT

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-27706_42-27704delinsAGC XP_016868399.1:n.42-27706_42-27704delinsAGC
XM_017012911.1:c.42-27706_42-27704delinsAGC XP_016868400.1:n.42-27706_42-27704delinsAGC
XR_001745121.1:n.473+35952_473+35954delinsAGC
XR_001745122.1:n.345-86376_345-86374delinsAGC
XR_001745123.1:n.473+35952_473+35954delinsAGC
XR_001745124.1:n.473+35952_473+35954delinsAGC
XR_001745125.1:n.473+35952_473+35954delinsAGC
XR_001745126.1:n.473+35952_473+35954delinsAGC
XR_001745127.1:n.345-27706_345-27704delinsAGC
XR_001745129.1:n.473+35952_473+35954delinsAGC
XR_001745130.1:n.473+35952_473+35954delinsAGC
XR_001745131.1:n.473+35952_473+35954delinsAGC
XR_001745132.1:n.473+35952_473+35954delinsAGC