Canonical Allele Identifier: CA1143595918
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995752T= , CM000663.2:g.196995752T= GRCh38
NC_000001.10:g.196964882T= , CM000663.1:g.196964882T= GRCh37
NC_000001.9:g.195231505T= NCBI36
NG_016365.1:g.23216T= , LRG_227:g.23216T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.388T= ENSP00000514393.1:p.Ser130=
ENST00000699467.1:n.712T=
ENST00000699468.1:c.-24-362T= ENSP00000514394.1:n.-24-362T=
ENST00000256785.5:c.643T= MANE Select ENSP00000256785.4:p.Ser215=
ENST00000256785.4:c.643T= ENSP00000256785.4:p.Ser215=
NM_030787.3:c.643T= , LRG_227t1:c.643T= NP_110414.1:p.Ser215=
XM_011510020.1:c.652T= XP_011508322.1:p.Ser218=
XM_011510020.2:c.652T= XP_011508322.1:p.Ser218=
NM_030787.4:c.643T= MANE Select NP_110414.1:p.Ser215=