Canonical Allele Identifier: CA1217885118

Gene: CFHR5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995948_196995950delinsTTA , CM000663.2:g.196995948_196995950delinsTTA	GRCh38
NC_000001.10:g.196965078_196965080delinsTTA , CM000663.1:g.196965078_196965080delinsTTA	GRCh37
NC_000001.9:g.195231701_195231703delinsTTA	NCBI36
NG_016365.1:g.23412_23414delinsTTA , LRG_227:g.23412_23414delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.535+49_535+51delinsTTA	ENSP00000514393.1:n.535+49_535+51delinsTTA
ENST00000699467.1:n.859+49_859+51delinsTTA
ENST00000699468.1:c.-24-166_-24-164delinsTTA	ENSP00000514394.1:n.-24-166_-24-164delinsTTA
ENST00000256785.5:c.790+49_790+51delinsTTA MANE Select	ENSP00000256785.4:n.790+49_790+51delinsTTA
ENST00000256785.4:c.790+49_790+51delinsTTA	ENSP00000256785.4:n.790+49_790+51delinsTTA
NM_030787.3:c.790+49_790+51delinsTTA , LRG_227t1:c.790+49_790+51delinsTTA	NP_110414.1:n.790+49_790+51delinsTTA
XM_011510020.1:c.799+49_799+51delinsTTA	XP_011508322.1:n.799+49_799+51delinsTTA
XM_011510020.2:c.799+49_799+51delinsTTA	XP_011508322.1:n.799+49_799+51delinsTTA
NM_030787.4:c.790+49_790+51delinsTTA MANE Select	NP_110414.1:n.790+49_790+51delinsTTA