Canonical Allele Identifier: CA1217885043
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995771A= , CM000663.2:g.196995771A= GRCh38
NC_000001.10:g.196964901A= , CM000663.1:g.196964901A= GRCh37
NC_000001.9:g.195231524A= NCBI36
NG_016365.1:g.23235A= , LRG_227:g.23235A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.407A= ENSP00000514393.1:p.Glu136=
ENST00000699467.1:n.731A=
ENST00000699468.1:c.-24-343A= ENSP00000514394.1:n.-24-343A=
ENST00000256785.5:c.662A= MANE Select ENSP00000256785.4:p.Glu221=
ENST00000256785.4:c.662A= ENSP00000256785.4:p.Glu221=
NM_030787.3:c.662A= , LRG_227t1:c.662A= NP_110414.1:p.Glu221=
XM_011510020.1:c.671A= XP_011508322.1:p.Glu224=
XM_011510020.2:c.671A= XP_011508322.1:p.Glu224=
NM_030787.4:c.662A= MANE Select NP_110414.1:p.Glu221=