Canonical Allele Identifier: CA2538312490
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283590_24283593del , CM000669.2:g.24283590_24283593del GRCh38
NC_000007.13:g.24323209_24323212del , CM000669.1:g.24323209_24323212del GRCh37
NC_000007.12:g.24289734_24289737del NCBI36
NG_016148.1:g.4403_4406del

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-27891_42-27888del XP_016868399.1:n.42-27891_42-27888del
XM_017012911.1:c.42-27891_42-27888del XP_016868400.1:n.42-27891_42-27888del
XR_001745121.1:n.473+35767_473+35770del
XR_001745122.1:n.345-86561_345-86558del
XR_001745123.1:n.473+35767_473+35770del
XR_001745124.1:n.473+35767_473+35770del
XR_001745125.1:n.473+35767_473+35770del
XR_001745126.1:n.473+35767_473+35770del
XR_001745127.1:n.345-27891_345-27888del
XR_001745129.1:n.473+35767_473+35770del
XR_001745130.1:n.473+35767_473+35770del
XR_001745131.1:n.473+35767_473+35770del
XR_001745132.1:n.473+35767_473+35770del