Canonical Allele Identifier: CA380021241

Gene: CD59

Linked Data

• MyVariant Identifiers: chr11:g.33738940C>A (hg19) ; chr11:g.33717394C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.33717394C>A , CM000673.2:g.33717394C>A	GRCh38
NC_000011.9:g.33738940C>A , CM000673.1:g.33738940C>A	GRCh37
NC_000011.8:g.33695516C>A	NCBI36
NG_008057.1:g.24085G>T , LRG_41:g.24085G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706436.1:c.138G>T	ENSP00000516379.1:p.Leu46Phe
ENST00000351554.8:c.145G>T	ENSP00000340210.3:p.Asp49Tyr
ENST00000395850.9:c.145G>T	ENSP00000379191.3:p.Asp49Tyr
ENST00000415002.7:c.145G>T	ENSP00000404822.2:p.Asp49Tyr
ENST00000426650.7:c.145G>T	ENSP00000402425.3:p.Asp49Tyr
ENST00000528700.2:c.145G>T	ENSP00000434617.2:p.Asp49Tyr
ENST00000533403.6:c.145G>T	ENSP00000436737.1:p.Asp49Tyr
ENST00000642928.2:c.145G>T MANE Select	ENSP00000494884.1:p.Asp49Tyr
ENST00000643183.1:c.145G>T	ENSP00000495784.1:p.Asp49Tyr
ENST00000651485.1:c.44G>T
ENST00000651785.1:c.145G>T	ENSP00000498879.1:p.Asp49Tyr
ENST00000652086.1:c.145G>T	ENSP00000498387.1:p.Asp49Tyr
ENST00000652678.1:c.145G>T	ENSP00000498448.1:p.Asp49Tyr
ENST00000351554.7:c.145G>T	ENSP00000340210.3:p.Asp49Tyr
ENST00000395850.7:c.145G>T	ENSP00000379191.3:p.Asp49Tyr
ENST00000415002.6:c.145G>T	ENSP00000404822.2:p.Asp49Tyr
ENST00000426650.6:c.145G>T	ENSP00000402425.2:p.Asp49Tyr
ENST00000437761.6:c.145G>T	ENSP00000410182.2:p.Asp49Tyr
ENST00000445143.6:c.145G>T	ENSP00000403511.2:p.Asp49Tyr
ENST00000525763.5:c.145G>T	ENSP00000435179.1:p.Asp49Tyr
ENST00000527577.5:c.145G>T	ENSP00000432942.1:p.Asp49Tyr
ENST00000527926.5:c.145G>T	ENSP00000437122.1:p.Asp49Tyr
ENST00000528700.1:c.145G>T	ENSP00000434617.1:p.Asp49Tyr
ENST00000528987.1:n.2218G>T
ENST00000533403.5:c.145G>T	ENSP00000436737.1:p.Asp49Tyr
ENST00000534312.5:c.145G>T	ENSP00000432362.1:p.Asp49Tyr
NM_000611.5:c.145G>T	NP_000602.1:p.Asp49Tyr
NM_001127223.1:c.145G>T	NP_001120695.1:p.Asp49Tyr
NM_001127225.1:c.145G>T	NP_001120697.1:p.Asp49Tyr
NM_001127226.1:c.145G>T	NP_001120698.1:p.Asp49Tyr
NM_001127227.1:c.145G>T	NP_001120699.1:p.Asp49Tyr
NM_203329.2:c.145G>T	NP_976074.1:p.Asp49Tyr
NM_203330.2:c.145G>T , LRG_41t1:c.145G>T	NP_976075.1:p.Asp49Tyr
NM_203331.2:c.145G>T	NP_976076.1:p.Asp49Tyr
NM_000611.6:c.145G>T MANE Select	NP_000602.1:p.Asp49Tyr
NM_001127225.2:c.145G>T	NP_001120697.1:p.Asp49Tyr
NM_001127226.2:c.145G>T	NP_001120698.1:p.Asp49Tyr
NM_001127227.2:c.145G>T	NP_001120699.1:p.Asp49Tyr
NM_203329.3:c.145G>T	NP_976074.1:p.Asp49Tyr
NM_203331.3:c.145G>T	NP_976076.1:p.Asp49Tyr