Canonical Allele Identifier: CA1217885041
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995767A= , CM000663.2:g.196995767A= GRCh38
NC_000001.10:g.196964897A= , CM000663.1:g.196964897A= GRCh37
NC_000001.9:g.195231520A= NCBI36
NG_016365.1:g.23231A= , LRG_227:g.23231A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.403A= ENSP00000514393.1:p.Lys135=
ENST00000699467.1:n.727A=
ENST00000699468.1:c.-24-347A= ENSP00000514394.1:n.-24-347A=
ENST00000256785.5:c.658A= MANE Select ENSP00000256785.4:p.Lys220=
ENST00000256785.4:c.658A= ENSP00000256785.4:p.Lys220=
NM_030787.3:c.658A= , LRG_227t1:c.658A= NP_110414.1:p.Lys220=
XM_011510020.1:c.667A= XP_011508322.1:p.Lys223=
XM_011510020.2:c.667A= XP_011508322.1:p.Lys223=
NM_030787.4:c.658A= MANE Select NP_110414.1:p.Lys220=