Canonical Allele Identifier: CA1217885115
Gene: CFHR5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995930G= , CM000663.2:g.196995930G= GRCh38
NC_000001.10:g.196965060G= , CM000663.1:g.196965060G= GRCh37
NC_000001.9:g.195231683G= NCBI36
NG_016365.1:g.23394G= , LRG_227:g.23394G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.535+31G= ENSP00000514393.1:n.535+31G=
ENST00000699467.1:n.859+31G=
ENST00000699468.1:c.-24-184G= ENSP00000514394.1:n.-24-184G=
ENST00000256785.5:c.790+31G= MANE Select ENSP00000256785.4:n.790+31G=
ENST00000256785.4:c.790+31G= ENSP00000256785.4:n.790+31G=
NM_030787.3:c.790+31G= , LRG_227t1:c.790+31G= NP_110414.1:n.790+31G=
XM_011510020.1:c.799+31G= XP_011508322.1:n.799+31G=
XM_011510020.2:c.799+31G= XP_011508322.1:n.799+31G=
NM_030787.4:c.790+31G= MANE Select NP_110414.1:n.790+31G=
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