Canonical Allele Identifier: CA639141828
Gene:

Linked Data

dbSNP Id: rs1490575545

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36130018_36130039del , CM000684.2:g.36130018_36130039del GRCh38
NC_000022.10:g.36526066_36526087del , CM000684.1:g.36526066_36526087del GRCh37
NC_000022.9:g.34856012_34856033del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_430441.2:n.1547+3123_1547+3144del
XR_938219.1:n.2897_2918del
XR_938220.1:n.2897_2918del
XR_938221.1:n.1471+3823_1471+3844del
XR_001755516.2:n.4759_4780del
XR_001755517.2:n.2986_3007del
XR_001755518.2:n.4759_4780del
XR_001755519.2:n.4759_4780del
XR_001755520.2:n.4759_4780del
XR_001755521.2:n.4759_4780del
XR_001755522.2:n.1637-2266_1637-2245del
XR_001755525.2:n.1637-685_1637-664del
XR_001755526.2:n.1637-2266_1637-2245del
XR_430441.4:n.1636+3123_1636+3144del