Canonical Allele Identifier: CA422956887

Gene: CD55

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207331160A>G , CM000663.2:g.207331160A>G	GRCh38
NC_000001.10:g.207504505A>G , CM000663.1:g.207504505A>G	GRCh37
NC_000001.9:g.205571128A>G	NCBI36
NG_007465.1:g.14689A>G , LRG_127:g.14689A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000574.5:c.717A>G MANE Select	NP_000565.1:p.Glu239=
ENST00000367064.9:c.717A>G MANE Select	ENSP00000356031.4:p.Glu239=
NM_000574.4:c.717A>G	NP_000565.1:p.Glu239=
NM_001114752.2:c.717A>G	NP_001108224.1:p.Glu239=
NM_001114752.3:c.717A>G	NP_001108224.1:p.Glu239=
NM_001300902.1:c.717A>G	NP_001287831.1:p.Glu239=
NM_001300902.2:c.717A>G	NP_001287831.1:p.Glu239=
NM_001300903.1:c.717A>G	NP_001287832.1:p.Glu239=
NM_001300903.2:c.717A>G	NP_001287832.1:p.Glu239=
NM_001300904.1:c.717A>G	NP_001287833.1:p.Glu239=
NM_001300904.2:c.717A>G	NP_001287833.1:p.Glu239=
NR_125349.1:n.1011A>G
NR_125349.2:n.805A>G
ENST00000314754.12:c.717A>G	ENSP00000316333.8:p.Glu239=
ENST00000343420.6:c.746A>G
ENST00000367063.6:c.717A>G	ENSP00000356030.2:p.Glu239=
ENST00000367064.7:c.717A>G	ENSP00000356031.3:p.Glu239=
ENST00000367067.8:c.717A>G	ENSP00000356034.5:p.Glu239=
ENST00000391921.8:c.525A>G	ENSP00000375788.4:p.Glu175=
ENST00000391921.9:c.525A>G	ENSP00000375788.4:p.Glu175=
ENST00000465534.5:n.332A>G
ENST00000476590.1:n.332A>G
ENST00000488171.5:n.796A>G
ENST00000488171.6:n.332A>G
ENST00000618707.2:c.221A>G
ENST00000635614.1:n.53A>G
ENST00000635614.2:c.59A>G
ENST00000644836.1:c.717A>G	ENSP00000495518.1:p.Glu239=
ENST00000645323.1:c.717A>G	ENSP00000496251.1:p.Glu239=
ENST00000695822.1:n.964A>G
ENST00000695823.1:c.664+4323A>G	ENSP00000512200.1:n.664+4323A>G
ENST00000695824.1:c.717A>G	ENSP00000512201.1:p.Glu239=
ENST00000695825.1:c.717A>G	ENSP00000512202.1:p.Glu239=
ENST00000695826.1:c.717A>G	ENSP00000512203.1:p.Glu239=
ENST00000695827.1:n.945A>G
ENST00000695828.1:c.664+4323A>G	ENSP00000512204.1:n.664+4323A>G
ENST00000695829.1:n.822A>G
XM_017000467.2:c.717A>G	XP_016855956.1:p.Glu239=