Canonical Allele Identifier: CA1694873419
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283741_24283742delinsGC , CM000669.2:g.24283741_24283742delinsGC GRCh38
NC_000007.13:g.24323360_24323361delinsGC , CM000669.1:g.24323360_24323361delinsGC GRCh37
NC_000007.12:g.24289885_24289886delinsGC NCBI36
NG_016148.1:g.4554_4555delinsGC

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-28043_42-28042delinsGC XP_016868399.1:n.42-28043_42-28042delinsG...
XM_017012911.1:c.42-28043_42-28042delinsGC XP_016868400.1:n.42-28043_42-28042delinsG...
XR_001745121.1:n.473+35615_473+35616delinsGC
XR_001745122.1:n.345-86713_345-86712delinsGC
XR_001745123.1:n.473+35615_473+35616delinsGC
XR_001745124.1:n.473+35615_473+35616delinsGC
XR_001745125.1:n.473+35615_473+35616delinsGC
XR_001745126.1:n.473+35615_473+35616delinsGC
XR_001745127.1:n.345-28043_345-28042delinsGC
XR_001745129.1:n.473+35615_473+35616delinsGC
XR_001745130.1:n.473+35615_473+35616delinsGC
XR_001745131.1:n.473+35615_473+35616delinsGC
XR_001745132.1:n.473+35615_473+35616delinsGC