Canonical Allele Identifier: CA1217885156
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996032A= , CM000663.2:g.196996032A= GRCh38
NC_000001.10:g.196965162A= , CM000663.1:g.196965162A= GRCh37
NC_000001.9:g.195231785A= NCBI36
NG_016365.1:g.23496A= , LRG_227:g.23496A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.546A= ENSP00000514393.1:p.Lys182=
ENST00000699467.1:n.870A=
ENST00000699468.1:c.-24-82A= ENSP00000514394.1:n.-24-82A=
ENST00000256785.5:c.801A= MANE Select ENSP00000256785.4:p.Lys267=
ENST00000256785.4:c.801A= ENSP00000256785.4:p.Lys267=
NM_030787.3:c.801A= , LRG_227t1:c.801A= NP_110414.1:p.Lys267=
XM_011510020.1:c.810A= XP_011508322.1:p.Lys270=
XM_011510020.2:c.810A= XP_011508322.1:p.Lys270=
NM_030787.4:c.801A= MANE Select NP_110414.1:p.Lys267=