Canonical Allele Identifier: CA1188689920

Gene: CD53

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110875308A= , CM000663.2:g.110875308A=	GRCh38
NC_000001.10:g.111417930A= , CM000663.1:g.111417930A=	GRCh37
NC_000001.9:g.111219453A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271324.6:c.-18+2060A= MANE Select	ENSP00000271324.5:n.-18+2060A=
ENST00000648608.1:c.-18+2060A=	ENSP00000497382.1:n.-18+2060A=
ENST00000271324.5:c.-18+2060A=	ENSP00000271324.5:n.-18+2060A=
ENST00000471220.5:n.66+2060A=
NM_000560.3:c.-18+2060A=	NP_000551.1:n.-18+2060A=
NM_001040033.1:c.-18+2060A=	NP_001035122.1:n.-18+2060A=
XM_006711053.2:c.-18+2060A=	XP_006711116.1:n.-18+2060A=
XM_011542447.1:c.-18+2060A=	XP_011540749.1:n.-18+2060A=
NM_001320638.1:c.-18+2060A=	NP_001307567.1:n.-18+2060A=
XM_024451057.1:c.-894+2060A=	XP_024306825.1:n.-894+2060A=
NM_000560.4:c.-18+2060A= MANE Select	NP_000551.1:n.-18+2060A=
NM_001040033.2:c.-18+2060A=	NP_001035122.1:n.-18+2060A=
NM_001320638.2:c.-18+2060A=	NP_001307567.1:n.-18+2060A=