Canonical Allele Identifier: CA2649656567

Gene: CFHR5

Linked Data

• gnomAD v4: 1-196995601-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995606del , CM000663.2:g.196995606del	GRCh38
NC_000001.10:g.196964736del , CM000663.1:g.196964736del	GRCh37
NC_000001.9:g.195231359del	NCBI36
NG_016365.1:g.23070del , LRG_227:g.23070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.353-111del	ENSP00000514393.1:n.353-111del
ENST00000699467.1:n.677-111del
ENST00000699468.1:c.-24-508del	ENSP00000514394.1:n.-24-508del
ENST00000256785.5:c.608-111del MANE Select	ENSP00000256785.4:n.608-111del
ENST00000256785.4:c.608-111del	ENSP00000256785.4:n.608-111del
NM_030787.3:c.608-111del , LRG_227t1:c.608-111del	NP_110414.1:n.608-111del
XM_011510020.1:c.617-111del	XP_011508322.1:n.617-111del
XM_011510020.2:c.617-111del	XP_011508322.1:n.617-111del
NM_030787.4:c.608-111del MANE Select	NP_110414.1:n.608-111del