Canonical Allele Identifier: CA10606451

Gene: FKRP

Linked Data

• ClinVar Variation Id: 289472
• ClinVar RCV Id: RCV000376960 ; RCV000473686
• dbSNP Id: rs755588907
• gnomAD v4: 19-46755845-G-A
• MyVariant Identifiers: chr19:g.47259102G>A (hg19) ; chr19:g.46755845G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46755845G>A , CM000681.2:g.46755845G>A	GRCh38
NC_000019.9:g.47259102G>A , CM000681.1:g.47259102G>A	GRCh37
NC_000019.8:g.51950942G>A	NCBI36
NG_008898.2:g.14800G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318584.10:c.395G>A MANE Select	ENSP00000326570.4:p.Gly132Glu
ENST00000318584.9:c.395G>A	ENSP00000326570.4:p.Gly132Glu
ENST00000391909.7:c.395G>A	ENSP00000375776.2:p.Gly132Glu
ENST00000593902.1:c.395G>A	ENSP00000470901.1:p.Gly132Glu
ENST00000594467.5:c.-35G>A	ENSP00000471971.1:n.-35G>A
ENST00000597339.5:n.247-5988G>A
ENST00000600646.5:n.247+7180G>A
ENST00000601299.5:c.395G>A	ENSP00000470103.1:p.Gly132Glu
NM_001039885.2:c.395G>A	NP_001034974.1:p.Gly132Glu
NM_024301.4:c.395G>A	NP_077277.1:p.Gly132Glu
XM_005259247.1:c.395G>A	XP_005259304.1:p.Gly132Glu
XM_005259248.1:c.395G>A	XP_005259305.1:p.Gly132Glu
XM_005259249.3:c.395G>A	XP_005259306.1:p.Gly132Glu
XM_005259250.3:c.395G>A	XP_005259307.1:p.Gly132Glu
XM_011527301.1:c.395G>A	XP_011525603.1:p.Gly132Glu
XM_011527302.1:c.395G>A	XP_011525604.1:p.Gly132Glu
XM_011527303.1:c.395G>A	XP_011525605.1:p.Gly132Glu
XM_011527304.1:c.395G>A	XP_011525606.1:p.Gly132Glu
XM_011527305.1:c.395G>A	XP_011525607.1:p.Gly132Glu
XM_011527306.1:c.395G>A	XP_011525608.1:p.Gly132Glu
XM_011527307.1:c.395G>A	XP_011525609.1:p.Gly132Glu
XM_005259247.2:c.395G>A	XP_005259304.1:p.Gly132Glu
XM_005259248.2:c.395G>A	XP_005259305.1:p.Gly132Glu
XM_005259249.4:c.395G>A	XP_005259306.1:p.Gly132Glu
XM_011527306.2:c.395G>A	XP_011525608.1:p.Gly132Glu
XM_017027297.2:c.395G>A	XP_016882786.1:p.Gly132Glu
XM_024451707.1:c.395G>A	XP_024307475.1:p.Gly132Glu
NM_001039885.3:c.395G>A	NP_001034974.1:p.Gly132Glu
NM_024301.5:c.395G>A MANE Select	NP_077277.1:p.Gly132Glu