Canonical Allele Identifier: CA1217885144
Gene: CFHR5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995995A= , CM000663.2:g.196995995A= GRCh38
NC_000001.10:g.196965125A= , CM000663.1:g.196965125A= GRCh37
NC_000001.9:g.195231748A= NCBI36
NG_016365.1:g.23459A= , LRG_227:g.23459A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.536-27A= ENSP00000514393.1:n.536-27A=
ENST00000699467.1:n.860-27A=
ENST00000699468.1:c.-24-119A= ENSP00000514394.1:n.-24-119A=
ENST00000256785.5:c.791-27A= MANE Select ENSP00000256785.4:n.791-27A=
ENST00000256785.4:c.791-27A= ENSP00000256785.4:n.791-27A=
NM_030787.3:c.791-27A= , LRG_227t1:c.791-27A= NP_110414.1:n.791-27A=
XM_011510020.1:c.800-27A= XP_011508322.1:n.800-27A=
XM_011510020.2:c.800-27A= XP_011508322.1:n.800-27A=
NM_030787.4:c.791-27A= MANE Select NP_110414.1:n.791-27A=
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