Canonical Allele Identifier: CA1143400413
Gene: CFHR5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995927A= , CM000663.2:g.196995927A= GRCh38
NC_000001.10:g.196965057A= , CM000663.1:g.196965057A= GRCh37
NC_000001.9:g.195231680A= NCBI36
NG_016365.1:g.23391A= , LRG_227:g.23391A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.535+28A= ENSP00000514393.1:n.535+28A=
ENST00000699467.1:n.859+28A=
ENST00000699468.1:c.-24-187A= ENSP00000514394.1:n.-24-187A=
ENST00000256785.5:c.790+28A= MANE Select ENSP00000256785.4:n.790+28A=
ENST00000256785.4:c.790+28A= ENSP00000256785.4:n.790+28A=
NM_030787.3:c.790+28A= , LRG_227t1:c.790+28A= NP_110414.1:n.790+28A=
XM_011510020.1:c.799+28A= XP_011508322.1:n.799+28A=
XM_011510020.2:c.799+28A= XP_011508322.1:n.799+28A=
NM_030787.4:c.790+28A= MANE Select NP_110414.1:n.790+28A=
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