Canonical Allele Identifier: CA1142182018
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995756A= , CM000663.2:g.196995756A= GRCh38
NC_000001.10:g.196964886A= , CM000663.1:g.196964886A= GRCh37
NC_000001.9:g.195231509A= NCBI36
NG_016365.1:g.23220A= , LRG_227:g.23220A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.392A= ENSP00000514393.1:p.Asn131=
ENST00000699467.1:n.716A=
ENST00000699468.1:c.-24-358A= ENSP00000514394.1:n.-24-358A=
ENST00000256785.5:c.647A= MANE Select ENSP00000256785.4:p.Asn216=
ENST00000256785.4:c.647A= ENSP00000256785.4:p.Asn216=
NM_030787.3:c.647A= , LRG_227t1:c.647A= NP_110414.1:p.Asn216=
XM_011510020.1:c.656A= XP_011508322.1:p.Asn219=
XM_011510020.2:c.656A= XP_011508322.1:p.Asn219=
NM_030787.4:c.647A= MANE Select NP_110414.1:p.Asn216=