Canonical Allele Identifier: CA344521602

Gene: CD55

Linked Data

• gnomAD v4: 1-207337226-T-G
• MyVariant Identifiers: chr1:g.207510571T>G (hg19) ; chr1:g.207337226T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207337226T>G , CM000663.2:g.207337226T>G	GRCh38
NC_000001.10:g.207510571T>G , CM000663.1:g.207510571T>G	GRCh37
NC_000001.9:g.205577194T>G	NCBI36
NG_007465.1:g.20755T>G , LRG_127:g.20755T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695822.1:n.1227-103T>G
ENST00000695823.1:c.791-103T>G	ENSP00000512200.1:n.791-103T>G
ENST00000695824.1:c.980-103T>G	ENSP00000512201.1:n.980-103T>G
ENST00000695825.1:c.980-103T>G	ENSP00000512202.1:n.980-103T>G
ENST00000695826.1:c.980-103T>G	ENSP00000512203.1:n.980-103T>G
ENST00000695827.1:n.1615T>G
ENST00000695828.1:c.791-103T>G	ENSP00000512204.1:n.791-103T>G
ENST00000695831.1:n.649T>G
ENST00000367064.9:c.980-103T>G MANE Select	ENSP00000356031.4:n.980-103T>G
ENST00000391921.9:c.788-103T>G	ENSP00000375788.4:n.788-103T>G
ENST00000488171.6:n.595-103T>G
ENST00000618707.2:c.484-103T>G
ENST00000635614.2:c.322-103T>G
ENST00000644836.1:c.980-103T>G	ENSP00000495518.1:n.980-103T>G
ENST00000645323.1:c.980-103T>G	ENSP00000496251.1:n.980-103T>G
ENST00000314754.12:c.980-103T>G	ENSP00000316333.8:n.980-103T>G
ENST00000367063.6:c.980-103T>G	ENSP00000356030.2:n.980-103T>G
ENST00000367064.7:c.980-103T>G	ENSP00000356031.3:n.980-103T>G
ENST00000367067.8:c.1384T>G	ENSP00000356034.5:p.Phe462Val
ENST00000391921.8:c.788-103T>G	ENSP00000375788.4:n.788-103T>G
ENST00000465534.5:n.1002T>G
ENST00000476590.1:n.1002T>G
ENST00000488171.5:n.1059-103T>G
ENST00000634386.1:n.66-103T>G
ENST00000635614.1:n.316-103T>G
NM_000574.4:c.980-103T>G	NP_000565.1:n.980-103T>G
NM_001114752.2:c.980-103T>G	NP_001108224.1:n.980-103T>G
NM_001300902.1:c.980-103T>G	NP_001287831.1:n.980-103T>G
NM_001300903.1:c.980-103T>G	NP_001287832.1:n.980-103T>G
NM_001300904.1:c.980-103T>G	NP_001287833.1:n.980-103T>G
NR_125349.1:n.1274-103T>G
XM_017000467.2:c.980-103T>G	XP_016855956.1:n.980-103T>G
NM_000574.5:c.980-103T>G MANE Select	NP_000565.1:n.980-103T>G
NM_001114752.3:c.980-103T>G	NP_001108224.1:n.980-103T>G
NM_001300902.2:c.980-103T>G	NP_001287831.1:n.980-103T>G
NM_001300903.2:c.980-103T>G	NP_001287832.1:n.980-103T>G
NM_001300904.2:c.980-103T>G	NP_001287833.1:n.980-103T>G
NR_125349.2:n.1068-103T>G