Canonical Allele Identifier: CA1217885088
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995889C= , CM000663.2:g.196995889C= GRCh38
NC_000001.10:g.196965019C= , CM000663.1:g.196965019C= GRCh37
NC_000001.9:g.195231642C= NCBI36
NG_016365.1:g.23353C= , LRG_227:g.23353C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.525C= ENSP00000514393.1:p.Pro175=
ENST00000699467.1:n.849C=
ENST00000699468.1:c.-24-225C= ENSP00000514394.1:n.-24-225C=
ENST00000256785.5:c.780C= MANE Select ENSP00000256785.4:p.Pro260=
ENST00000256785.4:c.780C= ENSP00000256785.4:p.Pro260=
NM_030787.3:c.780C= , LRG_227t1:c.780C= NP_110414.1:p.Pro260=
XM_011510020.1:c.789C= XP_011508322.1:p.Pro263=
XM_011510020.2:c.789C= XP_011508322.1:p.Pro263=
NM_030787.4:c.780C= MANE Select NP_110414.1:p.Pro260=