Canonical Allele Identifier: CA1143542265
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996062C= , CM000663.2:g.196996062C= GRCh38
NC_000001.10:g.196965192C= , CM000663.1:g.196965192C= GRCh37
NC_000001.9:g.195231815C= NCBI36
NG_016365.1:g.23526C= , LRG_227:g.23526C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.576C= ENSP00000514393.1:p.Tyr192=
ENST00000699467.1:n.900C=
ENST00000699468.1:c.-24-52C= ENSP00000514394.1:n.-24-52C=
ENST00000256785.5:c.831C= MANE Select ENSP00000256785.4:p.Tyr277=
ENST00000256785.4:c.831C= ENSP00000256785.4:p.Tyr277=
NM_030787.3:c.831C= , LRG_227t1:c.831C= NP_110414.1:p.Tyr277=
XM_011510020.1:c.840C= XP_011508322.1:p.Tyr280=
XM_011510020.2:c.840C= XP_011508322.1:p.Tyr280=
NM_030787.4:c.831C= MANE Select NP_110414.1:p.Tyr277=