Canonical Allele Identifier: CA1139970258
Gene: CD53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110875293C= , CM000663.2:g.110875293C= GRCh38
NC_000001.10:g.111417915C= , CM000663.1:g.111417915C= GRCh37
NC_000001.9:g.111219438C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000271324.6:c.-18+2045C= MANE Select ENSP00000271324.5:n.-18+2045C=
ENST00000648608.1:c.-18+2045C= ENSP00000497382.1:n.-18+2045C=
ENST00000271324.5:c.-18+2045C= ENSP00000271324.5:n.-18+2045C=
ENST00000471220.5:n.66+2045C=
NM_000560.3:c.-18+2045C= NP_000551.1:n.-18+2045C=
NM_001040033.1:c.-18+2045C= NP_001035122.1:n.-18+2045C=
XM_006711053.2:c.-18+2045C= XP_006711116.1:n.-18+2045C=
XM_011542447.1:c.-18+2045C= XP_011540749.1:n.-18+2045C=
NM_001320638.1:c.-18+2045C= NP_001307567.1:n.-18+2045C=
XM_024451057.1:c.-894+2045C= XP_024306825.1:n.-894+2045C=
NM_000560.4:c.-18+2045C= MANE Select NP_000551.1:n.-18+2045C=
NM_001040033.2:c.-18+2045C= NP_001035122.1:n.-18+2045C=
NM_001320638.2:c.-18+2045C= NP_001307567.1:n.-18+2045C=