Canonical Allele Identifier: CA1217885072
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995856A= , CM000663.2:g.196995856A= GRCh38
NC_000001.10:g.196964986A= , CM000663.1:g.196964986A= GRCh37
NC_000001.9:g.195231609A= NCBI36
NG_016365.1:g.23320A= , LRG_227:g.23320A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.492A= ENSP00000514393.1:p.Ile164=
ENST00000699467.1:n.816A=
ENST00000699468.1:c.-24-258A= ENSP00000514394.1:n.-24-258A=
ENST00000256785.5:c.747A= MANE Select ENSP00000256785.4:p.Ile249=
ENST00000256785.4:c.747A= ENSP00000256785.4:p.Ile249=
NM_030787.3:c.747A= , LRG_227t1:c.747A= NP_110414.1:p.Ile249=
XM_011510020.1:c.756A= XP_011508322.1:p.Ile252=
XM_011510020.2:c.756A= XP_011508322.1:p.Ile252=
NM_030787.4:c.747A= MANE Select NP_110414.1:p.Ile249=