Canonical Allele Identifier: CA1217885121
Gene: CFHR5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995953T= , CM000663.2:g.196995953T= GRCh38
NC_000001.10:g.196965083T= , CM000663.1:g.196965083T= GRCh37
NC_000001.9:g.195231706T= NCBI36
NG_016365.1:g.23417T= , LRG_227:g.23417T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.535+54T= ENSP00000514393.1:n.535+54T=
ENST00000699467.1:n.859+54T=
ENST00000699468.1:c.-24-161T= ENSP00000514394.1:n.-24-161T=
ENST00000256785.5:c.790+54T= MANE Select ENSP00000256785.4:n.790+54T=
ENST00000256785.4:c.790+54T= ENSP00000256785.4:n.790+54T=
NM_030787.3:c.790+54T= , LRG_227t1:c.790+54T= NP_110414.1:n.790+54T=
XM_011510020.1:c.799+54T= XP_011508322.1:n.799+54T=
XM_011510020.2:c.799+54T= XP_011508322.1:n.799+54T=
NM_030787.4:c.790+54T= MANE Select NP_110414.1:n.790+54T=
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