Canonical Allele Identifier: CA1694872927
Gene:

Linked Data

dbSNP Id: rs1787188408

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282763_24282765del , CM000669.2:g.24282763_24282765del GRCh38
NC_000007.13:g.24322382_24322384del , CM000669.1:g.24322382_24322384del GRCh37
NC_000007.12:g.24288907_24288909del NCBI36
NG_016148.1:g.3576_3578del

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-27064_42-27062del XP_016868399.1:n.42-27064_42-27062del
XM_017012911.1:c.42-27064_42-27062del XP_016868400.1:n.42-27064_42-27062del
XR_001745121.1:n.473+36594_473+36596del
XR_001745122.1:n.345-85734_345-85732del
XR_001745123.1:n.473+36594_473+36596del
XR_001745124.1:n.473+36594_473+36596del
XR_001745125.1:n.473+36594_473+36596del
XR_001745126.1:n.473+36594_473+36596del
XR_001745127.1:n.345-27064_345-27062del
XR_001745129.1:n.473+36594_473+36596del
XR_001745130.1:n.473+36594_473+36596del
XR_001745131.1:n.473+36594_473+36596del
XR_001745132.1:n.473+36594_473+36596del