Canonical Allele Identifier: CA1217885035
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995751C= , CM000663.2:g.196995751C= GRCh38
NC_000001.10:g.196964881C= , CM000663.1:g.196964881C= GRCh37
NC_000001.9:g.195231504C= NCBI36
NG_016365.1:g.23215C= , LRG_227:g.23215C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.387C= ENSP00000514393.1:p.Leu129=
ENST00000699467.1:n.711C=
ENST00000699468.1:c.-24-363C= ENSP00000514394.1:n.-24-363C=
ENST00000256785.5:c.642C= MANE Select ENSP00000256785.4:p.Leu214=
ENST00000256785.4:c.642C= ENSP00000256785.4:p.Leu214=
NM_030787.3:c.642C= , LRG_227t1:c.642C= NP_110414.1:p.Leu214=
XM_011510020.1:c.651C= XP_011508322.1:p.Leu217=
XM_011510020.2:c.651C= XP_011508322.1:p.Leu217=
NM_030787.4:c.642C= MANE Select NP_110414.1:p.Leu214=