Canonical Allele Identifier: CA1217885028
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995735G= , CM000663.2:g.196995735G= GRCh38
NC_000001.10:g.196964865G= , CM000663.1:g.196964865G= GRCh37
NC_000001.9:g.195231488G= NCBI36
NG_016365.1:g.23199G= , LRG_227:g.23199G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.371G= ENSP00000514393.1:p.Gly124=
ENST00000699467.1:n.695G=
ENST00000699468.1:c.-24-379G= ENSP00000514394.1:n.-24-379G=
ENST00000256785.5:c.626G= MANE Select ENSP00000256785.4:p.Gly209=
ENST00000256785.4:c.626G= ENSP00000256785.4:p.Gly209=
NM_030787.3:c.626G= , LRG_227t1:c.626G= NP_110414.1:p.Gly209=
XM_011510020.1:c.635G= XP_011508322.1:p.Gly212=
XM_011510020.2:c.635G= XP_011508322.1:p.Gly212=
NM_030787.4:c.626G= MANE Select NP_110414.1:p.Gly209=