Canonical Allele Identifier: CA2650257768

Gene: CD55

Linked Data

• gnomAD v4: 1-207337198-CCAAAAATTCACCACAGCAAAAGTTGCATTTACGCAGAGTCCTTCAGCAGCACGTAAGTCCACTAATGTACATTCCCCAGTGACTAATGGTCTCAAGAGTACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207337203_207337304del , CM000663.2:g.207337203_207337304del	GRCh38
NC_000001.10:g.207510548_207510649del , CM000663.1:g.207510548_207510649del	GRCh37
NC_000001.9:g.205577171_205577272del	NCBI36
NG_007465.1:g.20732_20833del , LRG_127:g.20732_20833del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695822.1:n.1227-126_1227-25del
ENST00000695823.1:c.791-126_791-25del	ENSP00000512200.1:n.791-126_791-25del
ENST00000695824.1:c.980-126_980-25del	ENSP00000512201.1:n.980-126_980-25del
ENST00000695825.1:c.980-126_980-25del	ENSP00000512202.1:n.980-126_980-25del
ENST00000695826.1:c.980-126_980-25del	ENSP00000512203.1:n.980-126_980-25del
ENST00000695827.1:n.1592_1693del
ENST00000695828.1:c.791-126_791-25del	ENSP00000512204.1:n.791-126_791-25del
ENST00000695831.1:n.626_727del
ENST00000367064.9:c.980-126_980-25del MANE Select	ENSP00000356031.4:n.980-126_980-25del
ENST00000391921.9:c.788-126_788-25del	ENSP00000375788.4:n.788-126_788-25del
ENST00000488171.6:n.595-126_595-25del
ENST00000618707.2:c.484-126_484-25del
ENST00000635614.2:c.322-126_322-25del
ENST00000644836.1:c.980-126_980-25del	ENSP00000495518.1:n.980-126_980-25del
ENST00000645323.1:c.980-126_980-25del	ENSP00000496251.1:n.980-126_980-25del
ENST00000314754.12:c.980-126_980-25del	ENSP00000316333.8:n.980-126_980-25del
ENST00000367063.6:c.980-126_980-25del	ENSP00000356030.2:n.980-126_980-25del
ENST00000367064.7:c.980-126_980-25del	ENSP00000356031.3:n.980-126_980-25del
ENST00000367067.8:c.1361_1462del	ENSP00000356034.5:p.Lys454_Gln487del
ENST00000391921.8:c.788-126_788-25del	ENSP00000375788.4:n.788-126_788-25del
ENST00000465534.5:n.979_1080del
ENST00000476590.1:n.979_1080del
ENST00000488171.5:n.1059-126_1059-25del
ENST00000634386.1:n.66-126_66-25del
ENST00000635614.1:n.316-126_316-25del
NM_000574.4:c.980-126_980-25del	NP_000565.1:n.980-126_980-25del
NM_001114752.2:c.980-126_980-25del	NP_001108224.1:n.980-126_980-25del
NM_001300902.1:c.980-126_980-25del	NP_001287831.1:n.980-126_980-25del
NM_001300903.1:c.980-126_980-25del	NP_001287832.1:n.980-126_980-25del
NM_001300904.1:c.980-126_980-25del	NP_001287833.1:n.980-126_980-25del
NR_125349.1:n.1274-126_1274-25del
XM_017000467.2:c.980-126_980-25del	XP_016855956.1:n.980-126_980-25del
NM_000574.5:c.980-126_980-25del MANE Select	NP_000565.1:n.980-126_980-25del
NM_001114752.3:c.980-126_980-25del	NP_001108224.1:n.980-126_980-25del
NM_001300902.2:c.980-126_980-25del	NP_001287831.1:n.980-126_980-25del
NM_001300903.2:c.980-126_980-25del	NP_001287832.1:n.980-126_980-25del
NM_001300904.2:c.980-126_980-25del	NP_001287833.1:n.980-126_980-25del
NR_125349.2:n.1068-126_1068-25del