Canonical Allele Identifier: CA406495045

Gene: FKRP

Linked Data

• gnomAD v4: 19-46755743-A-C
• MyVariant Identifiers: chr19:g.47259000A>C (hg19) ; chr19:g.46755743A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46755743A>C , CM000681.2:g.46755743A>C	GRCh38
NC_000019.9:g.47259000A>C , CM000681.1:g.47259000A>C	GRCh37
NC_000019.8:g.51950840A>C	NCBI36
NG_008898.2:g.14698A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318584.10:c.293A>C MANE Select	ENSP00000326570.4:p.Asn98Thr
ENST00000318584.9:c.293A>C	ENSP00000326570.4:p.Asn98Thr
ENST00000391909.7:c.293A>C	ENSP00000375776.2:p.Asn98Thr
ENST00000593800.5:c.293A>C	ENSP00000471209.1:p.Asn98Thr
ENST00000593902.1:c.293A>C	ENSP00000470901.1:p.Asn98Thr
ENST00000594467.5:c.-137A>C	ENSP00000471971.1:n.-137A>C
ENST00000596974.5:n.519A>C
ENST00000597339.5:n.247-6090A>C
ENST00000600005.5:c.293A>C	ENSP00000470335.1:p.Asn98Thr
ENST00000600227.5:c.293A>C	ENSP00000468825.1:p.Asn98Thr
ENST00000600646.5:n.247+7078A>C
ENST00000601299.5:c.293A>C	ENSP00000470103.1:p.Asn98Thr
NM_001039885.2:c.293A>C	NP_001034974.1:p.Asn98Thr
NM_024301.4:c.293A>C	NP_077277.1:p.Asn98Thr
XM_005259247.1:c.293A>C	XP_005259304.1:p.Asn98Thr
XM_005259248.1:c.293A>C	XP_005259305.1:p.Asn98Thr
XM_005259249.3:c.293A>C	XP_005259306.1:p.Asn98Thr
XM_005259250.3:c.293A>C	XP_005259307.1:p.Asn98Thr
XM_011527301.1:c.293A>C	XP_011525603.1:p.Asn98Thr
XM_011527302.1:c.293A>C	XP_011525604.1:p.Asn98Thr
XM_011527303.1:c.293A>C	XP_011525605.1:p.Asn98Thr
XM_011527304.1:c.293A>C	XP_011525606.1:p.Asn98Thr
XM_011527305.1:c.293A>C	XP_011525607.1:p.Asn98Thr
XM_011527306.1:c.293A>C	XP_011525608.1:p.Asn98Thr
XM_011527307.1:c.293A>C	XP_011525609.1:p.Asn98Thr
XM_005259247.2:c.293A>C	XP_005259304.1:p.Asn98Thr
XM_005259248.2:c.293A>C	XP_005259305.1:p.Asn98Thr
XM_005259249.4:c.293A>C	XP_005259306.1:p.Asn98Thr
XM_011527306.2:c.293A>C	XP_011525608.1:p.Asn98Thr
XM_017027297.2:c.293A>C	XP_016882786.1:p.Asn98Thr
XM_024451707.1:c.293A>C	XP_024307475.1:p.Asn98Thr
NM_001039885.3:c.293A>C	NP_001034974.1:p.Asn98Thr
NM_024301.5:c.293A>C MANE Select	NP_077277.1:p.Asn98Thr