Canonical Allele Identifier: CA344518048

Gene: CD55

Linked Data

• MyVariant Identifiers: chr1:g.207504587T>A (hg19) ; chr1:g.207331242T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207331242T>A , CM000663.2:g.207331242T>A	GRCh38
NC_000001.10:g.207504587T>A , CM000663.1:g.207504587T>A	GRCh37
NC_000001.9:g.205571210T>A	NCBI36
NG_007465.1:g.14771T>A , LRG_127:g.14771T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695822.1:n.1046T>A
ENST00000695823.1:c.664+4405T>A	ENSP00000512200.1:n.664+4405T>A
ENST00000695824.1:c.799T>A	ENSP00000512201.1:p.Cys267Ser
ENST00000695825.1:c.799T>A	ENSP00000512202.1:p.Cys267Ser
ENST00000695826.1:c.799T>A	ENSP00000512203.1:p.Cys267Ser
ENST00000695827.1:n.1027T>A
ENST00000695828.1:c.664+4405T>A	ENSP00000512204.1:n.664+4405T>A
ENST00000695829.1:n.904T>A
ENST00000367064.9:c.799T>A MANE Select	ENSP00000356031.4:p.Cys267Ser
ENST00000391921.9:c.607T>A	ENSP00000375788.4:p.Cys203Ser
ENST00000488171.6:n.414T>A
ENST00000618707.2:c.303T>A
ENST00000635614.2:c.141T>A
ENST00000644836.1:c.799T>A	ENSP00000495518.1:p.Cys267Ser
ENST00000645323.1:c.799T>A	ENSP00000496251.1:p.Cys267Ser
ENST00000314754.12:c.799T>A	ENSP00000316333.8:p.Cys267Ser
ENST00000343420.6:c.828T>A
ENST00000367063.6:c.799T>A	ENSP00000356030.2:p.Cys267Ser
ENST00000367064.7:c.799T>A	ENSP00000356031.3:p.Cys267Ser
ENST00000367067.8:c.799T>A	ENSP00000356034.5:p.Cys267Ser
ENST00000391921.8:c.607T>A	ENSP00000375788.4:p.Cys203Ser
ENST00000465534.5:n.414T>A
ENST00000476590.1:n.414T>A
ENST00000488171.5:n.878T>A
ENST00000635614.1:n.135T>A
NM_000574.4:c.799T>A	NP_000565.1:p.Cys267Ser
NM_001114752.2:c.799T>A	NP_001108224.1:p.Cys267Ser
NM_001300902.1:c.799T>A	NP_001287831.1:p.Cys267Ser
NM_001300903.1:c.799T>A	NP_001287832.1:p.Cys267Ser
NM_001300904.1:c.799T>A	NP_001287833.1:p.Cys267Ser
NR_125349.1:n.1093T>A
XM_017000467.2:c.799T>A	XP_016855956.1:p.Cys267Ser
NM_000574.5:c.799T>A MANE Select	NP_000565.1:p.Cys267Ser
NM_001114752.3:c.799T>A	NP_001108224.1:p.Cys267Ser
NM_001300902.2:c.799T>A	NP_001287831.1:p.Cys267Ser
NM_001300903.2:c.799T>A	NP_001287832.1:p.Cys267Ser
NM_001300904.2:c.799T>A	NP_001287833.1:p.Cys267Ser
NR_125349.2:n.887T>A