Canonical Allele Identifier: CA1694873462
Gene:

Linked Data

dbSNP Id: rs1787242954

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283797_24283806del , CM000669.2:g.24283797_24283806del GRCh38
NC_000007.13:g.24323416_24323425del , CM000669.1:g.24323416_24323425del GRCh37
NC_000007.12:g.24289941_24289950del NCBI36
NG_016148.1:g.4610_4619del

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-28107_42-28098del XP_016868399.1:n.42-28107_42-28098del
XM_017012911.1:c.42-28107_42-28098del XP_016868400.1:n.42-28107_42-28098del
XR_001745121.1:n.473+35551_473+35560del
XR_001745122.1:n.345-86777_345-86768del
XR_001745123.1:n.473+35551_473+35560del
XR_001745124.1:n.473+35551_473+35560del
XR_001745125.1:n.473+35551_473+35560del
XR_001745126.1:n.473+35551_473+35560del
XR_001745127.1:n.345-28107_345-28098del
XR_001745129.1:n.473+35551_473+35560del
XR_001745130.1:n.473+35551_473+35560del
XR_001745131.1:n.473+35551_473+35560del
XR_001745132.1:n.473+35551_473+35560del