Canonical Allele Identifier: CA2649656624
Gene: CFHR5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995910A>G , CM000663.2:g.196995910A>G GRCh38
NC_000001.10:g.196965040A>G , CM000663.1:g.196965040A>G GRCh37
NC_000001.9:g.195231663A>G NCBI36
NG_016365.1:g.23374A>G , LRG_227:g.23374A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.535+11A>G ENSP00000514393.1:n.535+11A>G
ENST00000699467.1:n.859+11A>G
ENST00000699468.1:c.-24-204A>G ENSP00000514394.1:n.-24-204A>G
ENST00000256785.5:c.790+11A>G MANE Select ENSP00000256785.4:n.790+11A>G
ENST00000256785.4:c.790+11A>G ENSP00000256785.4:n.790+11A>G
NM_030787.3:c.790+11A>G , LRG_227t1:c.790+11A>G NP_110414.1:n.790+11A>G
XM_011510020.1:c.799+11A>G XP_011508322.1:n.799+11A>G
XM_011510020.2:c.799+11A>G XP_011508322.1:n.799+11A>G
NM_030787.4:c.790+11A>G MANE Select NP_110414.1:n.790+11A>G