Canonical Allele Identifier: CA1099423992
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283576_24283578dup , CM000669.2:g.24283576_24283578dup GRCh38
NC_000007.13:g.24323195_24323197dup , CM000669.1:g.24323195_24323197dup GRCh37
NC_000007.12:g.24289720_24289722dup NCBI36
NG_016148.1:g.4389_4391dup

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-27879_42-27877dup XP_016868399.1:n.42-27879_42-27877dup
XM_017012911.1:c.42-27879_42-27877dup XP_016868400.1:n.42-27879_42-27877dup
XR_001745121.1:n.473+35779_473+35781dup
XR_001745122.1:n.345-86549_345-86547dup
XR_001745123.1:n.473+35779_473+35781dup
XR_001745124.1:n.473+35779_473+35781dup
XR_001745125.1:n.473+35779_473+35781dup
XR_001745126.1:n.473+35779_473+35781dup
XR_001745127.1:n.345-27879_345-27877dup
XR_001745129.1:n.473+35779_473+35781dup
XR_001745130.1:n.473+35779_473+35781dup
XR_001745131.1:n.473+35779_473+35781dup
XR_001745132.1:n.473+35779_473+35781dup