Canonical Allele Identifier: CA1217885186
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996095A= , CM000663.2:g.196996095A= GRCh38
NC_000001.10:g.196965225A= , CM000663.1:g.196965225A= GRCh37
NC_000001.9:g.195231848A= NCBI36
NG_016365.1:g.23559A= , LRG_227:g.23559A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.609A= ENSP00000514393.1:p.Gln203=
ENST00000699467.1:n.933A=
ENST00000699468.1:c.-24-19A= ENSP00000514394.1:n.-24-19A=
ENST00000256785.5:c.864A= MANE Select ENSP00000256785.4:p.Gln288=
ENST00000256785.4:c.864A= ENSP00000256785.4:p.Gln288=
NM_030787.3:c.864A= , LRG_227t1:c.864A= NP_110414.1:p.Gln288=
XM_011510020.1:c.873A= XP_011508322.1:p.Gln291=
XM_011510020.2:c.873A= XP_011508322.1:p.Gln291=
NM_030787.4:c.864A= MANE Select NP_110414.1:p.Gln288=