Canonical Allele Identifier: CA1217885141
Gene: CFHR5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995990G= , CM000663.2:g.196995990G= GRCh38
NC_000001.10:g.196965120G= , CM000663.1:g.196965120G= GRCh37
NC_000001.9:g.195231743G= NCBI36
NG_016365.1:g.23454G= , LRG_227:g.23454G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.536-32G= ENSP00000514393.1:n.536-32G=
ENST00000699467.1:n.860-32G=
ENST00000699468.1:c.-24-124G= ENSP00000514394.1:n.-24-124G=
ENST00000256785.5:c.791-32G= MANE Select ENSP00000256785.4:n.791-32G=
ENST00000256785.4:c.791-32G= ENSP00000256785.4:n.791-32G=
NM_030787.3:c.791-32G= , LRG_227t1:c.791-32G= NP_110414.1:n.791-32G=
XM_011510020.1:c.800-32G= XP_011508322.1:n.800-32G=
XM_011510020.2:c.800-32G= XP_011508322.1:n.800-32G=
NM_030787.4:c.791-32G= MANE Select NP_110414.1:n.791-32G=
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