Canonical Allele Identifier: CA1217884990

Gene: CFHR5

Linked Data

• dbSNP Id: rs1653968658

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995673_196995676dup , CM000663.2:g.196995673_196995676dup	GRCh38
NC_000001.10:g.196964803_196964806dup , CM000663.1:g.196964803_196964806dup	GRCh37
NC_000001.9:g.195231426_195231429dup	NCBI36
NG_016365.1:g.23137_23140dup , LRG_227:g.23137_23140dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.353-44_353-41dup	ENSP00000514393.1:n.353-44_353-41dup
ENST00000699467.1:n.677-44_677-41dup
ENST00000699468.1:c.-24-441_-24-438dup	ENSP00000514394.1:n.-24-441_-24-438dup
ENST00000256785.5:c.608-44_608-41dup MANE Select	ENSP00000256785.4:n.608-44_608-41dup
ENST00000256785.4:c.608-44_608-41dup	ENSP00000256785.4:n.608-44_608-41dup
NM_030787.3:c.608-44_608-41dup , LRG_227t1:c.608-44_608-41dup	NP_110414.1:n.608-44_608-41dup
XM_011510020.1:c.617-44_617-41dup	XP_011508322.1:n.617-44_617-41dup
XM_011510020.2:c.617-44_617-41dup	XP_011508322.1:n.617-44_617-41dup
NM_030787.4:c.608-44_608-41dup MANE Select	NP_110414.1:n.608-44_608-41dup