Canonical Allele Identifier: CA2202658639
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243390G= , CM000678.2:g.3243390G= GRCh38
NC_000016.9:g.3293390G= , CM000678.1:g.3293390G= GRCh37
NC_000016.8:g.3233391G= NCBI36
NG_007871.1:g.18238C= , LRG_190:g.18238C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1218C=
ENST00000219596.6:c.2097C= MANE Select ENSP00000219596.1:p.Tyr699=
ENST00000219596.5:c.2097C= ENSP00000219596.1:p.Tyr699=
ENST00000339854.8:c.1557C= ENSP00000339639.4:p.Tyr519=
ENST00000536379.5:c.1464C= ENSP00000445079.1:p.Tyr488=
ENST00000536980.5:c.*373C= ENSP00000444178.1:n.*373C=
ENST00000537682.5:c.*373C= ENSP00000438611.1:n.*373C=
ENST00000538326.5:c.*722C= ENSP00000437486.1:n.*722C=
ENST00000539145.5:c.1018C= ENSP00000444471.1:n.1018C=
ENST00000541159.5:c.1639C= ENSP00000438711.1:n.1639C=
ENST00000542898.5:c.*373C= ENSP00000444615.1:n.*373C=
ENST00000570511.5:c.1502C= ENSP00000458312.1:n.1502C=
ENST00000572244.5:c.787C= ENSP00000461186.1:n.787C=
ENST00000574583.5:c.869C= ENSP00000460269.1:n.869C=
ENST00000576315.5:c.902C= ENSP00000460551.1:n.902C=
ENST00000621655.1:c.1634C= ENSP00000481436.1:n.1634C=
NM_000243.2:c.2097C= , LRG_190t1:c.2097C= NP_000234.1:p.Tyr699=
NM_001198536.1:c.*301C= NP_001185465.1:n.*301C=
XM_017023236.2:c.2094C= XP_016878725.1:p.Tyr698=
NM_000243.3:c.2097C= MANE Select NP_000234.1:p.Tyr699=
NM_001198536.2:c.*301C= NP_001185465.2:n.*301C=