Canonical Allele Identifier: CA2202658664
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243432C= , CM000678.2:g.3243432C= GRCh38
NC_000016.9:g.3293432C= , CM000678.1:g.3293432C= GRCh37
NC_000016.8:g.3233433C= NCBI36
NG_007871.1:g.18196G= , LRG_190:g.18196G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1176G=
ENST00000219596.6:c.2055G= MANE Select ENSP00000219596.1:p.Glu685=
ENST00000219596.5:c.2055G= ENSP00000219596.1:p.Glu685=
ENST00000339854.8:c.1515G= ENSP00000339639.4:p.Glu505=
ENST00000536379.5:c.1422G= ENSP00000445079.1:p.Glu474=
ENST00000536980.5:c.*331G= ENSP00000444178.1:n.*331G=
ENST00000537682.5:c.*331G= ENSP00000438611.1:n.*331G=
ENST00000538326.5:c.*680G= ENSP00000437486.1:n.*680G=
ENST00000539145.5:c.976G= ENSP00000444471.1:n.976G=
ENST00000541159.5:c.1597G= ENSP00000438711.1:n.1597G=
ENST00000542898.5:c.*331G= ENSP00000444615.1:n.*331G=
ENST00000570511.5:c.1460G= ENSP00000458312.1:n.1460G=
ENST00000572244.5:c.745G= ENSP00000461186.1:n.745G=
ENST00000574583.5:c.827G= ENSP00000460269.1:n.827G=
ENST00000576315.5:c.860G= ENSP00000460551.1:n.860G=
ENST00000621655.1:c.1592G= ENSP00000481436.1:n.1592G=
NM_000243.2:c.2055G= , LRG_190t1:c.2055G= NP_000234.1:p.Glu685=
NM_001198536.1:c.*259G= NP_001185465.1:n.*259G=
XM_017023236.2:c.2052G= XP_016878725.1:p.Glu684=
NM_000243.3:c.2055G= MANE Select NP_000234.1:p.Glu685=
NM_001198536.2:c.*259G= NP_001185465.2:n.*259G=