Canonical Allele Identifier: CA646196874

Gene: CD53

Linked Data

• COSMIC: COSN9360574

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110875130T>G , CM000663.2:g.110875130T>G	GRCh38
NC_000001.10:g.111417752T>G , CM000663.1:g.111417752T>G	GRCh37
NC_000001.9:g.111219275T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271324.6:c.-18+1882T>G MANE Select	ENSP00000271324.5:n.-18+1882T>G
ENST00000648608.1:c.-18+1882T>G	ENSP00000497382.1:n.-18+1882T>G
ENST00000271324.5:c.-18+1882T>G	ENSP00000271324.5:n.-18+1882T>G
ENST00000471220.5:n.66+1882T>G
NM_000560.3:c.-18+1882T>G	NP_000551.1:n.-18+1882T>G
NM_001040033.1:c.-18+1882T>G	NP_001035122.1:n.-18+1882T>G
XM_006711053.2:c.-18+1882T>G	XP_006711116.1:n.-18+1882T>G
XM_011542447.1:c.-18+1882T>G	XP_011540749.1:n.-18+1882T>G
NM_001320638.1:c.-18+1882T>G	NP_001307567.1:n.-18+1882T>G
XM_024451057.1:c.-894+1882T>G	XP_024306825.1:n.-894+1882T>G
NM_000560.4:c.-18+1882T>G MANE Select	NP_000551.1:n.-18+1882T>G
NM_001040033.2:c.-18+1882T>G	NP_001035122.1:n.-18+1882T>G
NM_001320638.2:c.-18+1882T>G	NP_001307567.1:n.-18+1882T>G