Canonical Allele Identifier: CA1141581418

Gene: CD55

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_000574.5:c.261G= MANE Select	NP_000565.1:p.Trp87=
ENST00000367064.9:c.261G= MANE Select	ENSP00000356031.4:p.Trp87=
NM_000574.4:c.261G=	NP_000565.1:p.Trp87=
NM_001114752.2:c.261G=	NP_001108224.1:p.Trp87=
NM_001114752.3:c.261G=	NP_001108224.1:p.Trp87=
NM_001300902.1:c.261G=	NP_001287831.1:p.Trp87=
NM_001300902.2:c.261G=	NP_001287831.1:p.Trp87=
NM_001300903.1:c.261G=	NP_001287832.1:p.Trp87=
NM_001300903.2:c.261G=	NP_001287832.1:p.Trp87=
NM_001300904.1:c.261G=	NP_001287833.1:p.Trp87=
NM_001300904.2:c.261G=	NP_001287833.1:p.Trp87=
NR_125349.1:n.555G=
NR_125349.2:n.349G=
ENST00000314754.12:c.261G=	ENSP00000316333.8:p.Trp87=
ENST00000343420.6:c.290G=
ENST00000367063.6:c.261G=	ENSP00000356030.2:p.Trp87=
ENST00000367064.7:c.261G=	ENSP00000356031.3:p.Trp87=
ENST00000367067.8:c.261G=	ENSP00000356034.5:p.Trp87=
ENST00000391921.8:c.261G=	ENSP00000375788.4:p.Trp87=
ENST00000391921.9:c.261G=	ENSP00000375788.4:p.Trp87=
ENST00000488171.5:n.340G=
ENST00000644836.1:c.261G=	ENSP00000495518.1:p.Trp87=
ENST00000645323.1:c.261G=	ENSP00000496251.1:p.Trp87=
ENST00000695822.1:n.508G=
ENST00000695823.1:c.261G=	ENSP00000512200.1:p.Trp87=
ENST00000695824.1:c.261G=	ENSP00000512201.1:p.Trp87=
ENST00000695825.1:c.261G=	ENSP00000512202.1:p.Trp87=
ENST00000695826.1:c.261G=	ENSP00000512203.1:p.Trp87=
ENST00000695827.1:n.489G=
ENST00000695828.1:c.261G=	ENSP00000512204.1:p.Trp87=
ENST00000695829.1:n.366G=
ENST00000695830.1:n.79G=
XM_017000467.2:c.261G=	XP_016855956.1:p.Trp87=