Canonical Allele Identifier: CA1217885089
Gene: CFHR5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995890_196995891delinsAC , CM000663.2:g.196995890_196995891delinsAC GRCh38
NC_000001.10:g.196965020_196965021delinsAC , CM000663.1:g.196965020_196965021delinsAC GRCh37
NC_000001.9:g.195231643_195231644delinsAC NCBI36
NG_016365.1:g.23354_23355delinsAC , LRG_227:g.23354_23355delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.526_527delinsAC ENSP00000514393.1:p.Thr176=
ENST00000699467.1:n.850_851delinsAC
ENST00000699468.1:c.-24-224_-24-223delinsAC ENSP00000514394.1:n.-24-224_-24-223delinsAC
ENST00000256785.5:c.781_782delinsAC MANE Select ENSP00000256785.4:p.Thr261=
ENST00000256785.4:c.781_782delinsAC ENSP00000256785.4:p.Thr261=
NM_030787.3:c.781_782delinsAC , LRG_227t1:c.781_782delinsAC NP_110414.1:p.Thr261=
XM_011510020.1:c.790_791delinsAC XP_011508322.1:p.Thr264=
XM_011510020.2:c.790_791delinsAC XP_011508322.1:p.Thr264=
NM_030787.4:c.781_782delinsAC MANE Select NP_110414.1:p.Thr261=
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