Canonical Allele Identifier: CA1217885002
Gene: CFHR5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995691C= , CM000663.2:g.196995691C= GRCh38
NC_000001.10:g.196964821C= , CM000663.1:g.196964821C= GRCh37
NC_000001.9:g.195231444C= NCBI36
NG_016365.1:g.23155C= , LRG_227:g.23155C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.353-26C= ENSP00000514393.1:n.353-26C=
ENST00000699467.1:n.677-26C=
ENST00000699468.1:c.-24-423C= ENSP00000514394.1:n.-24-423C=
ENST00000256785.5:c.608-26C= MANE Select ENSP00000256785.4:n.608-26C=
ENST00000256785.4:c.608-26C= ENSP00000256785.4:n.608-26C=
NM_030787.3:c.608-26C= , LRG_227t1:c.608-26C= NP_110414.1:n.608-26C=
XM_011510020.1:c.617-26C= XP_011508322.1:n.617-26C=
XM_011510020.2:c.617-26C= XP_011508322.1:n.617-26C=
NM_030787.4:c.608-26C= MANE Select NP_110414.1:n.608-26C=
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