Canonical Allele Identifier: CA2339067362
Gene: FKRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46756243_46756244delinsCG , CM000681.2:g.46756243_46756244delinsCG GRCh38
NC_000019.9:g.47259500_47259501delinsCG , CM000681.1:g.47259500_47259501delinsCG GRCh37
NC_000019.8:g.51951340_51951341delinsCG NCBI36
NG_008898.2:g.15198_15199delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000318584.10:c.793_794delinsCG MANE Select ENSP00000326570.4:p.Arg265=
ENST00000318584.9:c.793_794delinsCG ENSP00000326570.4:p.Arg265=
ENST00000391909.7:c.793_794delinsCG ENSP00000375776.2:p.Arg265=
ENST00000597339.5:n.247-5590_247-5589delinsCG
ENST00000600646.5:n.247+7578_247+7579delinsCG
NM_001039885.2:c.793_794delinsCG NP_001034974.1:p.Arg265=
NM_024301.4:c.793_794delinsCG NP_077277.1:p.Arg265=
XM_005259247.1:c.793_794delinsCG XP_005259304.1:p.Arg265=
XM_005259248.1:c.793_794delinsCG XP_005259305.1:p.Arg265=
XM_005259249.3:c.793_794delinsCG XP_005259306.1:p.Arg265=
XM_005259250.3:c.793_794delinsCG XP_005259307.1:p.Arg265=
XM_011527301.1:c.793_794delinsCG XP_011525603.1:p.Arg265=
XM_011527302.1:c.793_794delinsCG XP_011525604.1:p.Arg265=
XM_011527303.1:c.793_794delinsCG XP_011525605.1:p.Arg265=
XM_011527304.1:c.793_794delinsCG XP_011525606.1:p.Arg265=
XM_011527305.1:c.793_794delinsCG XP_011525607.1:p.Arg265=
XM_011527306.1:c.793_794delinsCG XP_011525608.1:p.Arg265=
XM_011527307.1:c.793_794delinsCG XP_011525609.1:p.Arg265=
XM_005259247.2:c.793_794delinsCG XP_005259304.1:p.Arg265=
XM_005259248.2:c.793_794delinsCG XP_005259305.1:p.Arg265=
XM_005259249.4:c.793_794delinsCG XP_005259306.1:p.Arg265=
XM_011527306.2:c.793_794delinsCG XP_011525608.1:p.Arg265=
XM_017027297.2:c.793_794delinsCG XP_016882786.1:p.Arg265=
XM_024451707.1:c.793_794delinsCG XP_024307475.1:p.Arg265=
NM_001039885.3:c.793_794delinsCG NP_001034974.1:p.Arg265=
NM_024301.5:c.793_794delinsCG MANE Select NP_077277.1:p.Arg265=