Canonical Allele Identifier: CA1217885196
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996125A= , CM000663.2:g.196996125A= GRCh38
NC_000001.10:g.196965255A= , CM000663.1:g.196965255A= GRCh37
NC_000001.9:g.195231878A= NCBI36
NG_016365.1:g.23589A= , LRG_227:g.23589A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.639A= ENSP00000514393.1:p.Arg213=
ENST00000699467.1:n.963A=
ENST00000699468.1:c.-13A= ENSP00000514394.1:n.-13A=
ENST00000256785.5:c.894A= MANE Select ENSP00000256785.4:p.Arg298=
ENST00000256785.4:c.894A= ENSP00000256785.4:p.Arg298=
NM_030787.3:c.894A= , LRG_227t1:c.894A= NP_110414.1:p.Arg298=
XM_011510020.1:c.903A= XP_011508322.1:p.Arg301=
XM_011510020.2:c.903A= XP_011508322.1:p.Arg301=
NM_030787.4:c.894A= MANE Select NP_110414.1:p.Arg298=