Canonical Allele Identifier: CA126939
Gene: CD55 HGNC NCBI

Linked Data

ClinVar Variation Id: 16871
dbSNP Id: rs121909603

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207322542G>A , CM000663.2:g.207322542G>A GRCh38
NC_000001.10:g.207495887G>A , CM000663.1:g.207495887G>A GRCh37
NC_000001.9:g.205562510G>A NCBI36
NG_007465.1:g.6071G>A , LRG_127:g.6071G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695822.1:n.508G>A
ENST00000695823.1:c.261G>A ENSP00000512200.1:p.Trp87Ter
ENST00000695824.1:c.261G>A ENSP00000512201.1:p.Trp87Ter
ENST00000695825.1:c.261G>A ENSP00000512202.1:p.Trp87Ter
ENST00000695826.1:c.261G>A ENSP00000512203.1:p.Trp87Ter
ENST00000695827.1:n.489G>A
ENST00000695828.1:c.261G>A ENSP00000512204.1:p.Trp87Ter
ENST00000695829.1:n.366G>A
ENST00000695830.1:n.79G>A
ENST00000367064.9:c.261G>A MANE Select ENSP00000356031.4:p.Trp87Ter
ENST00000391921.9:c.261G>A ENSP00000375788.4:p.Trp87Ter
ENST00000644836.1:c.261G>A ENSP00000495518.1:p.Trp87Ter
ENST00000645323.1:c.261G>A ENSP00000496251.1:p.Trp87Ter
ENST00000314754.12:c.261G>A ENSP00000316333.8:p.Trp87Ter
ENST00000343420.6:c.290G>A
ENST00000367063.6:c.261G>A ENSP00000356030.2:p.Trp87Ter
ENST00000367064.7:c.261G>A ENSP00000356031.3:p.Trp87Ter
ENST00000367067.8:c.261G>A ENSP00000356034.5:p.Trp87Ter
ENST00000391921.8:c.261G>A ENSP00000375788.4:p.Trp87Ter
ENST00000488171.5:n.340G>A
NM_000574.4:c.261G>A NP_000565.1:p.Trp87Ter
NM_001114752.2:c.261G>A NP_001108224.1:p.Trp87Ter
NM_001300902.1:c.261G>A NP_001287831.1:p.Trp87Ter
NM_001300903.1:c.261G>A NP_001287832.1:p.Trp87Ter
NM_001300904.1:c.261G>A NP_001287833.1:p.Trp87Ter
NR_125349.1:n.555G>A
XM_017000467.2:c.261G>A XP_016855956.1:p.Trp87Ter
NM_000574.5:c.261G>A MANE Select NP_000565.1:p.Trp87Ter
NM_001114752.3:c.261G>A NP_001108224.1:p.Trp87Ter
NM_001300902.2:c.261G>A NP_001287831.1:p.Trp87Ter
NM_001300903.2:c.261G>A NP_001287832.1:p.Trp87Ter
NM_001300904.2:c.261G>A NP_001287833.1:p.Trp87Ter
NR_125349.2:n.349G>A