Canonical Allele Identifier: CA1367911

Gene: CD55

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207322429G>T , CM000663.2:g.207322429G>T	GRCh38
NC_000001.10:g.207495774G>T , CM000663.1:g.207495774G>T	GRCh37
NC_000001.9:g.205562397G>T	NCBI36
NG_007465.1:g.5958G>T , LRG_127:g.5958G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000574.5:c.148G>T MANE Select	NP_000565.1:p.Glu50Ter
ENST00000367064.9:c.148G>T MANE Select	ENSP00000356031.4:p.Glu50Ter
NM_000574.4:c.148G>T	NP_000565.1:p.Glu50Ter
NM_001114752.2:c.148G>T	NP_001108224.1:p.Glu50Ter
NM_001114752.3:c.148G>T	NP_001108224.1:p.Glu50Ter
NM_001300902.1:c.148G>T	NP_001287831.1:p.Glu50Ter
NM_001300902.2:c.148G>T	NP_001287831.1:p.Glu50Ter
NM_001300903.1:c.148G>T	NP_001287832.1:p.Glu50Ter
NM_001300903.2:c.148G>T	NP_001287832.1:p.Glu50Ter
NM_001300904.1:c.148G>T	NP_001287833.1:p.Glu50Ter
NM_001300904.2:c.148G>T	NP_001287833.1:p.Glu50Ter
NR_125349.1:n.442G>T
NR_125349.2:n.236G>T
ENST00000314754.12:c.148G>T	ENSP00000316333.8:p.Glu50Ter
ENST00000343420.6:c.177G>T
ENST00000367063.6:c.148G>T	ENSP00000356030.2:p.Glu50Ter
ENST00000367064.7:c.148G>T	ENSP00000356031.3:p.Glu50Ter
ENST00000367067.8:c.148G>T	ENSP00000356034.5:p.Glu50Ter
ENST00000391921.8:c.148G>T	ENSP00000375788.4:p.Glu50Ter
ENST00000391921.9:c.148G>T	ENSP00000375788.4:p.Glu50Ter
ENST00000488171.5:n.227G>T
ENST00000644836.1:c.148G>T	ENSP00000495518.1:p.Glu50Ter
ENST00000645323.1:c.148G>T	ENSP00000496251.1:p.Glu50Ter
ENST00000695822.1:n.395G>T
ENST00000695823.1:c.148G>T	ENSP00000512200.1:p.Glu50Ter
ENST00000695824.1:c.148G>T	ENSP00000512201.1:p.Glu50Ter
ENST00000695825.1:c.148G>T	ENSP00000512202.1:p.Glu50Ter
ENST00000695826.1:c.148G>T	ENSP00000512203.1:p.Glu50Ter
ENST00000695827.1:n.376G>T
ENST00000695828.1:c.148G>T	ENSP00000512204.1:p.Glu50Ter
ENST00000695829.1:n.253G>T
XM_017000467.2:c.148G>T	XP_016855956.1:p.Glu50Ter