Canonical Allele Identifier: CA1217885006
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995696T= , CM000663.2:g.196995696T= GRCh38
NC_000001.10:g.196964826T= , CM000663.1:g.196964826T= GRCh37
NC_000001.9:g.195231449T= NCBI36
NG_016365.1:g.23160T= , LRG_227:g.23160T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.353-21T= ENSP00000514393.1:n.353-21T=
ENST00000699467.1:n.677-21T=
ENST00000699468.1:c.-24-418T= ENSP00000514394.1:n.-24-418T=
ENST00000256785.5:c.608-21T= MANE Select ENSP00000256785.4:n.608-21T=
ENST00000256785.4:c.608-21T= ENSP00000256785.4:n.608-21T=
NM_030787.3:c.608-21T= , LRG_227t1:c.608-21T= NP_110414.1:n.608-21T=
XM_011510020.1:c.617-21T= XP_011508322.1:n.617-21T=
XM_011510020.2:c.617-21T= XP_011508322.1:n.617-21T=
NM_030787.4:c.608-21T= MANE Select NP_110414.1:n.608-21T=