Canonical Allele Identifier: CA2202660578
Gene: MEFV HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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