Canonical Allele Identifier: CA344004352
Gene: CFHR5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995720A>C , CM000663.2:g.196995720A>C GRCh38
NC_000001.10:g.196964850A>C , CM000663.1:g.196964850A>C GRCh37
NC_000001.9:g.195231473A>C NCBI36
NG_016365.1:g.23184A>C , LRG_227:g.23184A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.356A>C ENSP00000514393.1:p.Gln119Pro
ENST00000699467.1:n.680A>C
ENST00000699468.1:c.-24-394A>C ENSP00000514394.1:n.-24-394A>C
ENST00000256785.5:c.611A>C MANE Select ENSP00000256785.4:p.Gln204Pro
ENST00000256785.4:c.611A>C ENSP00000256785.4:p.Gln204Pro
NM_030787.3:c.611A>C , LRG_227t1:c.611A>C NP_110414.1:p.Gln204Pro
XM_011510020.1:c.620A>C XP_011508322.1:p.Gln207Pro
XM_011510020.2:c.620A>C XP_011508322.1:p.Gln207Pro
NM_030787.4:c.611A>C MANE Select NP_110414.1:p.Gln204Pro