Canonical Allele Identifier: CA1217885049
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995789A= , CM000663.2:g.196995789A= GRCh38
NC_000001.10:g.196964919A= , CM000663.1:g.196964919A= GRCh37
NC_000001.9:g.195231542A= NCBI36
NG_016365.1:g.23253A= , LRG_227:g.23253A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.425A= ENSP00000514393.1:p.Tyr142=
ENST00000699467.1:n.749A=
ENST00000699468.1:c.-24-325A= ENSP00000514394.1:n.-24-325A=
ENST00000256785.5:c.680A= MANE Select ENSP00000256785.4:p.Tyr227=
ENST00000256785.4:c.680A= ENSP00000256785.4:p.Tyr227=
NM_030787.3:c.680A= , LRG_227t1:c.680A= NP_110414.1:p.Tyr227=
XM_011510020.1:c.689A= XP_011508322.1:p.Tyr230=
XM_011510020.2:c.689A= XP_011508322.1:p.Tyr230=
NM_030787.4:c.680A= MANE Select NP_110414.1:p.Tyr227=