Canonical Allele Identifier: CA1217885031
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995744C= , CM000663.2:g.196995744C= GRCh38
NC_000001.10:g.196964874C= , CM000663.1:g.196964874C= GRCh37
NC_000001.9:g.195231497C= NCBI36
NG_016365.1:g.23208C= , LRG_227:g.23208C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.380C= ENSP00000514393.1:p.Pro127=
ENST00000699467.1:n.704C=
ENST00000699468.1:c.-24-370C= ENSP00000514394.1:n.-24-370C=
ENST00000256785.5:c.635C= MANE Select ENSP00000256785.4:p.Pro212=
ENST00000256785.4:c.635C= ENSP00000256785.4:p.Pro212=
NM_030787.3:c.635C= , LRG_227t1:c.635C= NP_110414.1:p.Pro212=
XM_011510020.1:c.644C= XP_011508322.1:p.Pro215=
XM_011510020.2:c.644C= XP_011508322.1:p.Pro215=
NM_030787.4:c.635C= MANE Select NP_110414.1:p.Pro212=