Canonical Allele Identifier: CA1217885055
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995799T= , CM000663.2:g.196995799T= GRCh38
NC_000001.10:g.196964929T= , CM000663.1:g.196964929T= GRCh37
NC_000001.9:g.195231552T= NCBI36
NG_016365.1:g.23263T= , LRG_227:g.23263T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.435T= ENSP00000514393.1:p.Asn145=
ENST00000699467.1:n.759T=
ENST00000699468.1:c.-24-315T= ENSP00000514394.1:n.-24-315T=
ENST00000256785.5:c.690T= MANE Select ENSP00000256785.4:p.Asn230=
ENST00000256785.4:c.690T= ENSP00000256785.4:p.Asn230=
NM_030787.3:c.690T= , LRG_227t1:c.690T= NP_110414.1:p.Asn230=
XM_011510020.1:c.699T= XP_011508322.1:p.Asn233=
XM_011510020.2:c.699T= XP_011508322.1:p.Asn233=
NM_030787.4:c.690T= MANE Select NP_110414.1:p.Asn230=