Canonical Allele Identifier: CA2202658671
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243445G= , CM000678.2:g.3243445G= GRCh38
NC_000016.9:g.3293445G= , CM000678.1:g.3293445G= GRCh37
NC_000016.8:g.3233446G= NCBI36
NG_007871.1:g.18183C= , LRG_190:g.18183C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1163C=
ENST00000219596.6:c.2042C= MANE Select ENSP00000219596.1:p.Thr681=
ENST00000219596.5:c.2042C= ENSP00000219596.1:p.Thr681=
ENST00000339854.8:c.1502C= ENSP00000339639.4:p.Thr501=
ENST00000536379.5:c.1409C= ENSP00000445079.1:p.Thr470=
ENST00000536980.5:c.*318C= ENSP00000444178.1:n.*318C=
ENST00000537682.5:c.*318C= ENSP00000438611.1:n.*318C=
ENST00000538326.5:c.*667C= ENSP00000437486.1:n.*667C=
ENST00000539145.5:c.963C= ENSP00000444471.1:n.963C=
ENST00000541159.5:c.1584C= ENSP00000438711.1:n.1584C=
ENST00000542898.5:c.*318C= ENSP00000444615.1:n.*318C=
ENST00000570511.5:c.1447C= ENSP00000458312.1:n.1447C=
ENST00000572244.5:c.732C= ENSP00000461186.1:n.732C=
ENST00000574583.5:c.814C= ENSP00000460269.1:n.814C=
ENST00000576315.5:c.847C= ENSP00000460551.1:n.847C=
ENST00000621655.1:c.1579C= ENSP00000481436.1:n.1579C=
NM_000243.2:c.2042C= , LRG_190t1:c.2042C= NP_000234.1:p.Thr681=
NM_001198536.1:c.*246C= NP_001185465.1:n.*246C=
XM_017023236.2:c.2039C= XP_016878725.1:p.Thr680=
NM_000243.3:c.2042C= MANE Select NP_000234.1:p.Thr681=
NM_001198536.2:c.*246C= NP_001185465.2:n.*246C=