Canonical Allele Identifier: CA2574104914

Gene: CFHR5

Linked Data

• gnomAD v4: 1-196995695-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995695A>T , CM000663.2:g.196995695A>T	GRCh38
NC_000001.10:g.196964825A>T , CM000663.1:g.196964825A>T	GRCh37
NC_000001.9:g.195231448A>T	NCBI36
NG_016365.1:g.23159A>T , LRG_227:g.23159A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.353-22A>T	ENSP00000514393.1:n.353-22A>T
ENST00000699467.1:n.677-22A>T
ENST00000699468.1:c.-24-419A>T	ENSP00000514394.1:n.-24-419A>T
ENST00000256785.5:c.608-22A>T MANE Select	ENSP00000256785.4:n.608-22A>T
ENST00000256785.4:c.608-22A>T	ENSP00000256785.4:n.608-22A>T
NM_030787.3:c.608-22A>T , LRG_227t1:c.608-22A>T	NP_110414.1:n.608-22A>T
XM_011510020.1:c.617-22A>T	XP_011508322.1:n.617-22A>T
XM_011510020.2:c.617-22A>T	XP_011508322.1:n.617-22A>T
NM_030787.4:c.608-22A>T MANE Select	NP_110414.1:n.608-22A>T