Canonical Allele Identifier: CA1217885143
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995993T= , CM000663.2:g.196995993T= GRCh38
NC_000001.10:g.196965123T= , CM000663.1:g.196965123T= GRCh37
NC_000001.9:g.195231746T= NCBI36
NG_016365.1:g.23457T= , LRG_227:g.23457T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.536-29T= ENSP00000514393.1:n.536-29T=
ENST00000699467.1:n.860-29T=
ENST00000699468.1:c.-24-121T= ENSP00000514394.1:n.-24-121T=
ENST00000256785.5:c.791-29T= MANE Select ENSP00000256785.4:n.791-29T=
ENST00000256785.4:c.791-29T= ENSP00000256785.4:n.791-29T=
NM_030787.3:c.791-29T= , LRG_227t1:c.791-29T= NP_110414.1:n.791-29T=
XM_011510020.1:c.800-29T= XP_011508322.1:n.800-29T=
XM_011510020.2:c.800-29T= XP_011508322.1:n.800-29T=
NM_030787.4:c.791-29T= MANE Select NP_110414.1:n.791-29T=