Canonical Allele Identifier: CA1217885033
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995746C= , CM000663.2:g.196995746C= GRCh38
NC_000001.10:g.196964876C= , CM000663.1:g.196964876C= GRCh37
NC_000001.9:g.195231499C= NCBI36
NG_016365.1:g.23210C= , LRG_227:g.23210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.382C= ENSP00000514393.1:p.Gln128=
ENST00000699467.1:n.706C=
ENST00000699468.1:c.-24-368C= ENSP00000514394.1:n.-24-368C=
ENST00000256785.5:c.637C= MANE Select ENSP00000256785.4:p.Gln213=
ENST00000256785.4:c.637C= ENSP00000256785.4:p.Gln213=
NM_030787.3:c.637C= , LRG_227t1:c.637C= NP_110414.1:p.Gln213=
XM_011510020.1:c.646C= XP_011508322.1:p.Gln216=
XM_011510020.2:c.646C= XP_011508322.1:p.Gln216=
NM_030787.4:c.637C= MANE Select NP_110414.1:p.Gln213=