Canonical Allele Identifier: CA493383629

Gene: MEFV

Linked Data

• ClinVar Variation Id: 2102386
• ClinVar RCV Id: RCV003019493
• dbSNP Id: rs1958952568
• MyVariant Identifiers: chr16:g.3297052C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247052C>T , CM000678.2:g.3247052C>T	GRCh38
NC_000016.9:g.3297052C>T , CM000678.1:g.3297052C>T	GRCh37
NC_000016.8:g.3237053C>T	NCBI36
NG_007871.1:g.14576G>A , LRG_190:g.14576G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000219596.6:c.1551G>A MANE Select	ENSP00000219596.1:p.Glu517=
ENST00000219596.5:c.1551G>A	ENSP00000219596.1:p.Glu517=
ENST00000339854.8:c.1011G>A	ENSP00000339639.4:p.Glu337=
ENST00000536379.5:c.918G>A	ENSP00000445079.1:p.Glu306=
ENST00000536980.5:c.918G>A	ENSP00000444178.1:p.Glu306=
ENST00000537682.5:c.1551G>A	ENSP00000438611.1:p.Glu517=
ENST00000538326.5:c.*176G>A	ENSP00000437486.1:n.*176G>A
ENST00000539145.5:c.472G>A	ENSP00000444471.1:n.472G>A
ENST00000539154.1:n.916G>A
ENST00000541159.5:c.918G>A	ENSP00000438711.1:p.Glu306=
ENST00000542898.5:c.1644G>A	ENSP00000444615.1:p.Glu548=
ENST00000570511.5:c.1105G>A	ENSP00000458312.1:n.1105G>A
ENST00000572244.5:c.278-505G>A	ENSP00000461186.1:n.278-505G>A
ENST00000574583.5:c.472G>A	ENSP00000460269.1:n.472G>A
ENST00000576315.5:c.472G>A	ENSP00000460551.1:n.472G>A
ENST00000621655.1:c.918G>A	ENSP00000481436.1:p.Glu306=
NM_000243.2:c.1551G>A , LRG_190t1:c.1551G>A	NP_000234.1:p.Glu517=
NM_001198536.1:c.918G>A	NP_001185465.1:p.Glu306=
XM_017023236.2:c.1548G>A	XP_016878725.1:p.Glu516=
XR_001751903.1:n.1740G>A
NM_000243.3:c.1551G>A MANE Select	NP_000234.1:p.Glu517=
NM_001198536.2:c.918G>A	NP_001185465.2:p.Glu306=