Canonical Allele Identifier: CA1143687652
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995699A= , CM000663.2:g.196995699A= GRCh38
NC_000001.10:g.196964829A= , CM000663.1:g.196964829A= GRCh37
NC_000001.9:g.195231452A= NCBI36
NG_016365.1:g.23163A= , LRG_227:g.23163A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.353-18A= ENSP00000514393.1:n.353-18A=
ENST00000699467.1:n.677-18A=
ENST00000699468.1:c.-24-415A= ENSP00000514394.1:n.-24-415A=
ENST00000256785.5:c.608-18A= MANE Select ENSP00000256785.4:n.608-18A=
ENST00000256785.4:c.608-18A= ENSP00000256785.4:n.608-18A=
NM_030787.3:c.608-18A= , LRG_227t1:c.608-18A= NP_110414.1:n.608-18A=
XM_011510020.1:c.617-18A= XP_011508322.1:n.617-18A=
XM_011510020.2:c.617-18A= XP_011508322.1:n.617-18A=
NM_030787.4:c.608-18A= MANE Select NP_110414.1:n.608-18A=