Canonical Allele Identifier: CA1010880314
Gene: CFHR5 HGNC NCBI

Linked Data

dbSNP Id: rs1653982202

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996047_196996048dup , CM000663.2:g.196996047_196996048dup GRCh38
NC_000001.10:g.196965177_196965178dup , CM000663.1:g.196965177_196965178dup GRCh37
NC_000001.9:g.195231800_195231801dup NCBI36
NG_016365.1:g.23511_23512dup , LRG_227:g.23511_23512dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.561_562dup ENSP00000514393.1:p.Pro188HisfsTer24
ENST00000699467.1:n.885_886dup
ENST00000699468.1:c.-24-67_-24-66dup ENSP00000514394.1:n.-24-67_-24-66dup
ENST00000256785.5:c.816_817dup MANE Select ENSP00000256785.4:p.Pro273HisfsTer24
ENST00000256785.4:c.816_817dup ENSP00000256785.4:p.Pro273HisfsTer24
NM_030787.3:c.816_817dup , LRG_227t1:c.816_817dup NP_110414.1:p.Pro273HisfsTer24
XM_011510020.1:c.825_826dup XP_011508322.1:p.Pro276HisfsTer24
XM_011510020.2:c.825_826dup XP_011508322.1:p.Pro276HisfsTer24
NM_030787.4:c.816_817dup MANE Select NP_110414.1:p.Pro273HisfsTer24