Canonical Allele Identifier: CA1694873442

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283769_24283770delinsTC , CM000669.2:g.24283769_24283770delinsTC	GRCh38
NC_000007.13:g.24323388_24323389delinsTC , CM000669.1:g.24323388_24323389delinsTC	GRCh37
NC_000007.12:g.24289913_24289914delinsTC	NCBI36
NG_016148.1:g.4582_4583delinsTC

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-28071_42-28070delinsGA	XP_016868399.1:n.42-28071_42-28070delinsGA
XM_017012911.1:c.42-28071_42-28070delinsGA	XP_016868400.1:n.42-28071_42-28070delinsGA
XR_001745121.1:n.473+35587_473+35588delinsGA
XR_001745122.1:n.345-86741_345-86740delinsGA
XR_001745123.1:n.473+35587_473+35588delinsGA
XR_001745124.1:n.473+35587_473+35588delinsGA
XR_001745125.1:n.473+35587_473+35588delinsGA
XR_001745126.1:n.473+35587_473+35588delinsGA
XR_001745127.1:n.345-28071_345-28070delinsGA
XR_001745129.1:n.473+35587_473+35588delinsGA
XR_001745130.1:n.473+35587_473+35588delinsGA
XR_001745131.1:n.473+35587_473+35588delinsGA
XR_001745132.1:n.473+35587_473+35588delinsGA