Canonical Allele Identifier: CA2580614918

Gene: FKRP

Linked Data

• ClinVar Variation Id: 1368772
• ClinVar RCV Id: RCV001867668
• dbSNP Id: rs2122607119

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46755483_46755485del , CM000681.2:g.46755483_46755485del	GRCh38
NC_000019.9:g.47258740_47258742del , CM000681.1:g.47258740_47258742del	GRCh37
NC_000019.8:g.51950580_51950582del	NCBI36
NG_008898.2:g.14438_14440del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318584.10:c.33_35del MANE Select	ENSP00000326570.4:p.Ala12del
ENST00000318584.9:c.33_35del	ENSP00000326570.4:p.Ala12del
ENST00000391909.7:c.33_35del	ENSP00000375776.2:p.Ala12del
ENST00000593800.5:c.33_35del	ENSP00000471209.1:p.Ala12del
ENST00000593875.5:c.33_35del	ENSP00000470297.1:p.Ala12del
ENST00000593902.1:c.33_35del	ENSP00000470901.1:p.Ala12del
ENST00000594467.5:c.-345-52_-345-50del	ENSP00000471971.1:n.-345-52_-345-50del
ENST00000595570.5:c.33_35del	ENSP00000470929.1:p.Ala12del
ENST00000595868.5:c.33_35del	ENSP00000471573.1:p.Ala12del
ENST00000596460.5:c.33_35del	ENSP00000469373.1:p.Ala12del
ENST00000596974.5:n.311-52_311-50del
ENST00000597313.5:c.33_35del	ENSP00000472370.1:p.Ala12del
ENST00000597339.5:n.247-6350_247-6348del
ENST00000598271.5:c.33_35del	ENSP00000471088.1:p.Ala12del
ENST00000600005.5:c.33_35del	ENSP00000470335.1:p.Ala12del
ENST00000600227.5:c.33_35del	ENSP00000468825.1:p.Ala12del
ENST00000600629.5:c.33_35del	ENSP00000470096.1:p.Ala12del
ENST00000600646.5:n.247+6818_247+6820del
ENST00000600834.5:c.33_35del	ENSP00000470024.1:p.Ala12del
ENST00000601299.5:c.33_35del	ENSP00000470103.1:p.Ala12del
ENST00000602181.5:c.33_35del	ENSP00000472981.1:p.Ala12del
ENST00000602250.5:c.33_35del	ENSP00000472807.1:p.Ala12del
NM_001039885.2:c.33_35del	NP_001034974.1:p.Ala12del
NM_024301.4:c.33_35del	NP_077277.1:p.Ala12del
XM_005259247.1:c.33_35del	XP_005259304.1:p.Ala12del
XM_005259248.1:c.33_35del	XP_005259305.1:p.Ala12del
XM_005259249.3:c.33_35del	XP_005259306.1:p.Ala12del
XM_005259250.3:c.33_35del	XP_005259307.1:p.Ala12del
XM_011527301.1:c.33_35del	XP_011525603.1:p.Ala12del
XM_011527302.1:c.33_35del	XP_011525604.1:p.Ala12del
XM_011527303.1:c.33_35del	XP_011525605.1:p.Ala12del
XM_011527304.1:c.33_35del	XP_011525606.1:p.Ala12del
XM_011527305.1:c.33_35del	XP_011525607.1:p.Ala12del
XM_011527306.1:c.33_35del	XP_011525608.1:p.Ala12del
XM_011527307.1:c.33_35del	XP_011525609.1:p.Ala12del
XM_005259247.2:c.33_35del	XP_005259304.1:p.Ala12del
XM_005259248.2:c.33_35del	XP_005259305.1:p.Ala12del
XM_005259249.4:c.33_35del	XP_005259306.1:p.Ala12del
XM_011527306.2:c.33_35del	XP_011525608.1:p.Ala12del
XM_017027297.2:c.33_35del	XP_016882786.1:p.Ala12del
XM_024451707.1:c.33_35del	XP_024307475.1:p.Ala12del
NM_001039885.3:c.33_35del	NP_001034974.1:p.Ala12del
NM_024301.5:c.33_35del MANE Select	NP_077277.1:p.Ala12del