Canonical Allele Identifier: CA1367945

Gene: CD55

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207322569T>G , CM000663.2:g.207322569T>G	GRCh38
NC_000001.10:g.207495914T>G , CM000663.1:g.207495914T>G	GRCh37
NC_000001.9:g.205562537T>G	NCBI36
NG_007465.1:g.6098T>G , LRG_127:g.6098T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000574.5:c.286+2T>G MANE Select	NP_000565.1:n.286+2T>G
ENST00000367064.9:c.286+2T>G MANE Select	ENSP00000356031.4:n.286+2T>G
NM_000574.4:c.286+2T>G	NP_000565.1:n.286+2T>G
NM_001114752.2:c.286+2T>G	NP_001108224.1:n.286+2T>G
NM_001114752.3:c.286+2T>G	NP_001108224.1:n.286+2T>G
NM_001300902.1:c.286+2T>G	NP_001287831.1:n.286+2T>G
NM_001300902.2:c.286+2T>G	NP_001287831.1:n.286+2T>G
NM_001300903.1:c.286+2T>G	NP_001287832.1:n.286+2T>G
NM_001300903.2:c.286+2T>G	NP_001287832.1:n.286+2T>G
NM_001300904.1:c.286+2T>G	NP_001287833.1:n.286+2T>G
NM_001300904.2:c.286+2T>G	NP_001287833.1:n.286+2T>G
NR_125349.1:n.580+2T>G
NR_125349.2:n.374+2T>G
ENST00000314754.12:c.286+2T>G	ENSP00000316333.8:n.286+2T>G
ENST00000343420.6:c.315+2T>G
ENST00000367063.6:c.286+2T>G	ENSP00000356030.2:n.286+2T>G
ENST00000367064.7:c.286+2T>G	ENSP00000356031.3:n.286+2T>G
ENST00000367067.8:c.286+2T>G	ENSP00000356034.5:n.286+2T>G
ENST00000391921.8:c.286+2T>G	ENSP00000375788.4:n.286+2T>G
ENST00000391921.9:c.286+2T>G	ENSP00000375788.4:n.286+2T>G
ENST00000488171.5:n.365+2T>G
ENST00000644836.1:c.286+2T>G	ENSP00000495518.1:n.286+2T>G
ENST00000645323.1:c.286+2T>G	ENSP00000496251.1:n.286+2T>G
ENST00000695822.1:n.533+2T>G
ENST00000695823.1:c.286+2T>G	ENSP00000512200.1:n.286+2T>G
ENST00000695824.1:c.286+2T>G	ENSP00000512201.1:n.286+2T>G
ENST00000695825.1:c.286+2T>G	ENSP00000512202.1:n.286+2T>G
ENST00000695826.1:c.286+2T>G	ENSP00000512203.1:n.286+2T>G
ENST00000695827.1:n.514+2T>G
ENST00000695828.1:c.286+2T>G	ENSP00000512204.1:n.286+2T>G
ENST00000695829.1:n.391+2T>G
ENST00000695830.1:n.104+2T>G
XM_017000467.2:c.286+2T>G	XP_016855956.1:n.286+2T>G