Canonical Allele Identifier: CA2682049018
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291901_24291903del , CM000669.2:g.24291901_24291903del GRCh38
NC_000007.13:g.24331520_24331522del , CM000669.1:g.24331520_24331522del GRCh37
NC_000007.12:g.24298045_24298047del NCBI36
NG_016148.1:g.12714_12716del

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.41+27456_41+27458del XP_016868399.1:n.41+27456_41+27458del
XM_017012911.1:c.41+27456_41+27458del XP_016868400.1:n.41+27456_41+27458del
XR_001745121.1:n.473+27456_473+27458del
XR_001745122.1:n.345-94872_345-94870del
XR_001745123.1:n.473+27456_473+27458del
XR_001745124.1:n.473+27456_473+27458del
XR_001745125.1:n.473+27456_473+27458del
XR_001745126.1:n.473+27456_473+27458del
XR_001745127.1:n.345-36202_345-36200del
XR_001745129.1:n.473+27456_473+27458del
XR_001745130.1:n.473+27456_473+27458del
XR_001745131.1:n.473+27456_473+27458del
XR_001745132.1:n.473+27456_473+27458del