Canonical Allele Identifier: CA1217885032
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995745T= , CM000663.2:g.196995745T= GRCh38
NC_000001.10:g.196964875T= , CM000663.1:g.196964875T= GRCh37
NC_000001.9:g.195231498T= NCBI36
NG_016365.1:g.23209T= , LRG_227:g.23209T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.381T= ENSP00000514393.1:p.Pro127=
ENST00000699467.1:n.705T=
ENST00000699468.1:c.-24-369T= ENSP00000514394.1:n.-24-369T=
ENST00000256785.5:c.636T= MANE Select ENSP00000256785.4:p.Pro212=
ENST00000256785.4:c.636T= ENSP00000256785.4:p.Pro212=
NM_030787.3:c.636T= , LRG_227t1:c.636T= NP_110414.1:p.Pro212=
XM_011510020.1:c.645T= XP_011508322.1:p.Pro215=
XM_011510020.2:c.645T= XP_011508322.1:p.Pro215=
NM_030787.4:c.636T= MANE Select NP_110414.1:p.Pro212=