Canonical Allele Identifier: CA1143358665
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996057G= , CM000663.2:g.196996057G= GRCh38
NC_000001.10:g.196965187G= , CM000663.1:g.196965187G= GRCh37
NC_000001.9:g.195231810G= NCBI36
NG_016365.1:g.23521G= , LRG_227:g.23521G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.571G= ENSP00000514393.1:p.Glu191=
ENST00000699467.1:n.895G=
ENST00000699468.1:c.-24-57G= ENSP00000514394.1:n.-24-57G=
ENST00000256785.5:c.826G= MANE Select ENSP00000256785.4:p.Glu276=
ENST00000256785.4:c.826G= ENSP00000256785.4:p.Glu276=
NM_030787.3:c.826G= , LRG_227t1:c.826G= NP_110414.1:p.Glu276=
XM_011510020.1:c.835G= XP_011508322.1:p.Glu279=
XM_011510020.2:c.835G= XP_011508322.1:p.Glu279=
NM_030787.4:c.826G= MANE Select NP_110414.1:p.Glu276=