Canonical Allele Identifier: CA1694873241
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283442_24283443delinsTC , CM000669.2:g.24283442_24283443delinsTC GRCh38
NC_000007.13:g.24323061_24323062delinsTC , CM000669.1:g.24323061_24323062delinsTC GRCh37
NC_000007.12:g.24289586_24289587delinsTC NCBI36
NG_016148.1:g.4255_4256delinsTC

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-27744_42-27743delinsGA XP_016868399.1:n.42-27744_42-27743delinsGA
XM_017012911.1:c.42-27744_42-27743delinsGA XP_016868400.1:n.42-27744_42-27743delinsGA
XR_001745121.1:n.473+35914_473+35915delinsGA
XR_001745122.1:n.345-86414_345-86413delinsGA
XR_001745123.1:n.473+35914_473+35915delinsGA
XR_001745124.1:n.473+35914_473+35915delinsGA
XR_001745125.1:n.473+35914_473+35915delinsGA
XR_001745126.1:n.473+35914_473+35915delinsGA
XR_001745127.1:n.345-27744_345-27743delinsGA
XR_001745129.1:n.473+35914_473+35915delinsGA
XR_001745130.1:n.473+35914_473+35915delinsGA
XR_001745131.1:n.473+35914_473+35915delinsGA
XR_001745132.1:n.473+35914_473+35915delinsGA