Canonical Allele Identifier: CA1217885182
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996088C= , CM000663.2:g.196996088C= GRCh38
NC_000001.10:g.196965218C= , CM000663.1:g.196965218C= GRCh37
NC_000001.9:g.195231841C= NCBI36
NG_016365.1:g.23552C= , LRG_227:g.23552C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.602C= ENSP00000514393.1:p.Pro201=
ENST00000699467.1:n.926C=
ENST00000699468.1:c.-24-26C= ENSP00000514394.1:n.-24-26C=
ENST00000256785.5:c.857C= MANE Select ENSP00000256785.4:p.Pro286=
ENST00000256785.4:c.857C= ENSP00000256785.4:p.Pro286=
NM_030787.3:c.857C= , LRG_227t1:c.857C= NP_110414.1:p.Pro286=
XM_011510020.1:c.866C= XP_011508322.1:p.Pro289=
XM_011510020.2:c.866C= XP_011508322.1:p.Pro289=
NM_030787.4:c.857C= MANE Select NP_110414.1:p.Pro286=