Canonical Allele Identifier: CA2696602293

Gene: CD53

Linked Data

• dbSNP Id: rs2101035257

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110875085_110875112del , CM000663.2:g.110875085_110875112del	GRCh38
NC_000001.10:g.111417707_111417734del , CM000663.1:g.111417707_111417734del	GRCh37
NC_000001.9:g.111219230_111219257del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271324.6:c.-18+1837_-18+1864del MANE Select	ENSP00000271324.5:n.-18+1837_-18+1864del
ENST00000648608.1:c.-18+1837_-18+1864del	ENSP00000497382.1:n.-18+1837_-18+1864del
ENST00000271324.5:c.-18+1837_-18+1864del	ENSP00000271324.5:n.-18+1837_-18+1864del
ENST00000471220.5:n.66+1837_66+1864del
NM_000560.3:c.-18+1837_-18+1864del	NP_000551.1:n.-18+1837_-18+1864del
NM_001040033.1:c.-18+1837_-18+1864del	NP_001035122.1:n.-18+1837_-18+1864del
XM_006711053.2:c.-18+1837_-18+1864del	XP_006711116.1:n.-18+1837_-18+1864del
XM_011542447.1:c.-18+1837_-18+1864del	XP_011540749.1:n.-18+1837_-18+1864del
NM_001320638.1:c.-18+1837_-18+1864del	NP_001307567.1:n.-18+1837_-18+1864del
XM_024451057.1:c.-894+1837_-894+1864del	XP_024306825.1:n.-894+1837_-894+1864del
NM_000560.4:c.-18+1837_-18+1864del MANE Select	NP_000551.1:n.-18+1837_-18+1864del
NM_001040033.2:c.-18+1837_-18+1864del	NP_001035122.1:n.-18+1837_-18+1864del
NM_001320638.2:c.-18+1837_-18+1864del	NP_001307567.1:n.-18+1837_-18+1864del