Canonical Allele Identifier: CA1217884955

Gene: CFHR5

Linked Data

• dbSNP Id: rs1653966816

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995585_196995586insT , CM000663.2:g.196995585_196995586insT	GRCh38
NC_000001.10:g.196964715_196964716insT , CM000663.1:g.196964715_196964716insT	GRCh37
NC_000001.9:g.195231338_195231339insT	NCBI36
NG_016365.1:g.23049_23050insT , LRG_227:g.23049_23050insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.353-132_353-131insT	ENSP00000514393.1:n.353-132_353-131insT
ENST00000699467.1:n.677-132_677-131insT
ENST00000699468.1:c.-24-529_-24-528insT	ENSP00000514394.1:n.-24-529_-24-528insT
ENST00000256785.5:c.608-132_608-131insT MANE Select	ENSP00000256785.4:n.608-132_608-131insT
ENST00000256785.4:c.608-132_608-131insT	ENSP00000256785.4:n.608-132_608-131insT
NM_030787.3:c.608-132_608-131insT , LRG_227t1:c.608-132_608-131insT	NP_110414.1:n.608-132_608-131insT
XM_011510020.1:c.617-132_617-131insT	XP_011508322.1:n.617-132_617-131insT
XM_011510020.2:c.617-132_617-131insT	XP_011508322.1:n.617-132_617-131insT
NM_030787.4:c.608-132_608-131insT MANE Select	NP_110414.1:n.608-132_608-131insT