Canonical Allele Identifier: CA1694873395
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283708_24283709delinsGC , CM000669.2:g.24283708_24283709delinsGC GRCh38
NC_000007.13:g.24323327_24323328delinsGC , CM000669.1:g.24323327_24323328delinsGC GRCh37
NC_000007.12:g.24289852_24289853delinsGC NCBI36
NG_016148.1:g.4521_4522delinsGC

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-28010_42-28009delinsGC XP_016868399.1:n.42-28010_42-28009delinsG...
XM_017012911.1:c.42-28010_42-28009delinsGC XP_016868400.1:n.42-28010_42-28009delinsG...
XR_001745121.1:n.473+35648_473+35649delinsGC
XR_001745122.1:n.345-86680_345-86679delinsGC
XR_001745123.1:n.473+35648_473+35649delinsGC
XR_001745124.1:n.473+35648_473+35649delinsGC
XR_001745125.1:n.473+35648_473+35649delinsGC
XR_001745126.1:n.473+35648_473+35649delinsGC
XR_001745127.1:n.345-28010_345-28009delinsGC
XR_001745129.1:n.473+35648_473+35649delinsGC
XR_001745130.1:n.473+35648_473+35649delinsGC
XR_001745131.1:n.473+35648_473+35649delinsGC
XR_001745132.1:n.473+35648_473+35649delinsGC