Canonical Allele Identifier: CA1188689893

Gene: CD53

Linked Data

• dbSNP Id: rs1656077396

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110875247T>C , CM000663.2:g.110875247T>C	GRCh38
NC_000001.10:g.111417869T>C , CM000663.1:g.111417869T>C	GRCh37
NC_000001.9:g.111219392T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271324.6:c.-18+1999T>C MANE Select	ENSP00000271324.5:n.-18+1999T>C
ENST00000648608.1:c.-18+1999T>C	ENSP00000497382.1:n.-18+1999T>C
ENST00000271324.5:c.-18+1999T>C	ENSP00000271324.5:n.-18+1999T>C
ENST00000471220.5:n.66+1999T>C
NM_000560.3:c.-18+1999T>C	NP_000551.1:n.-18+1999T>C
NM_001040033.1:c.-18+1999T>C	NP_001035122.1:n.-18+1999T>C
XM_006711053.2:c.-18+1999T>C	XP_006711116.1:n.-18+1999T>C
XM_011542447.1:c.-18+1999T>C	XP_011540749.1:n.-18+1999T>C
NM_001320638.1:c.-18+1999T>C	NP_001307567.1:n.-18+1999T>C
XM_024451057.1:c.-894+1999T>C	XP_024306825.1:n.-894+1999T>C
NM_000560.4:c.-18+1999T>C MANE Select	NP_000551.1:n.-18+1999T>C
NM_001040033.2:c.-18+1999T>C	NP_001035122.1:n.-18+1999T>C
NM_001320638.2:c.-18+1999T>C	NP_001307567.1:n.-18+1999T>C