Canonical Allele Identifier: CA1694873489
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283833_24283834delinsTC , CM000669.2:g.24283833_24283834delinsTC GRCh38
NC_000007.13:g.24323452_24323453delinsTC , CM000669.1:g.24323452_24323453delinsTC GRCh37
NC_000007.12:g.24289977_24289978delinsTC NCBI36
NG_016148.1:g.4646_4647delinsTC

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-28135_42-28134delinsGA XP_016868399.1:n.42-28135_42-28134delinsGA
XM_017012911.1:c.42-28135_42-28134delinsGA XP_016868400.1:n.42-28135_42-28134delinsGA
XR_001745121.1:n.473+35523_473+35524delinsGA
XR_001745122.1:n.345-86805_345-86804delinsGA
XR_001745123.1:n.473+35523_473+35524delinsGA
XR_001745124.1:n.473+35523_473+35524delinsGA
XR_001745125.1:n.473+35523_473+35524delinsGA
XR_001745126.1:n.473+35523_473+35524delinsGA
XR_001745127.1:n.345-28135_345-28134delinsGA
XR_001745129.1:n.473+35523_473+35524delinsGA
XR_001745130.1:n.473+35523_473+35524delinsGA
XR_001745131.1:n.473+35523_473+35524delinsGA
XR_001745132.1:n.473+35523_473+35524delinsGA