Canonical Allele Identifier: CA2202658623
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243367G= , CM000678.2:g.3243367G= GRCh38
NC_000016.9:g.3293367G= , CM000678.1:g.3293367G= GRCh37
NC_000016.8:g.3233368G= NCBI36
NG_007871.1:g.18261C= , LRG_190:g.18261C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1241C=
ENST00000219596.6:c.2120C= MANE Select ENSP00000219596.1:p.Thr707=
ENST00000219596.5:c.2120C= ENSP00000219596.1:p.Thr707=
ENST00000339854.8:c.1580C= ENSP00000339639.4:p.Thr527=
ENST00000536379.5:c.1487C= ENSP00000445079.1:p.Thr496=
ENST00000536980.5:c.*396C= ENSP00000444178.1:n.*396C=
ENST00000537682.5:c.*396C= ENSP00000438611.1:n.*396C=
ENST00000538326.5:c.*745C= ENSP00000437486.1:n.*745C=
ENST00000539145.5:c.1041C= ENSP00000444471.1:n.1041C=
ENST00000541159.5:c.1662C= ENSP00000438711.1:n.1662C=
ENST00000542898.5:c.*396C= ENSP00000444615.1:n.*396C=
ENST00000570511.5:c.1525C= ENSP00000458312.1:n.1525C=
ENST00000572244.5:c.810C= ENSP00000461186.1:n.810C=
ENST00000574583.5:c.892C= ENSP00000460269.1:n.892C=
ENST00000576315.5:c.925C= ENSP00000460551.1:n.925C=
ENST00000621655.1:c.1657C= ENSP00000481436.1:n.1657C=
NM_000243.2:c.2120C= , LRG_190t1:c.2120C= NP_000234.1:p.Thr707=
NM_001198536.1:c.*324C= NP_001185465.1:n.*324C=
XM_017023236.2:c.2117C= XP_016878725.1:p.Thr706=
NM_000243.3:c.2120C= MANE Select NP_000234.1:p.Thr707=
NM_001198536.2:c.*324C= NP_001185465.2:n.*324C=