Canonical Allele Identifier: CA2202658560

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243256G= , CM000678.2:g.3243256G=	GRCh38
NC_000016.9:g.3293256G= , CM000678.1:g.3293256G=	GRCh37
NC_000016.8:g.3233257G=	NCBI36
NG_007871.1:g.18372C= , LRG_190:g.18372C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1352C=
ENST00000219596.6:c.2231C= MANE Select	ENSP00000219596.1:p.Ala744=
ENST00000219596.5:c.2231C=	ENSP00000219596.1:p.Ala744=
ENST00000339854.8:c.1691C=	ENSP00000339639.4:p.Ala564=
ENST00000536379.5:c.1598C=	ENSP00000445079.1:p.Ala533=
ENST00000536980.5:c.*507C=	ENSP00000444178.1:n.*507C=
ENST00000537682.5:c.*507C=	ENSP00000438611.1:n.*507C=
ENST00000538326.5:c.*856C=	ENSP00000437486.1:n.*856C=
ENST00000539145.5:c.1152C=	ENSP00000444471.1:n.1152C=
ENST00000541159.5:c.1773C=	ENSP00000438711.1:n.1773C=
ENST00000542898.5:c.*507C=	ENSP00000444615.1:n.*507C=
ENST00000570511.5:c.1636C=	ENSP00000458312.1:n.1636C=
ENST00000572244.5:c.921C=	ENSP00000461186.1:n.921C=
ENST00000574583.5:c.1003C=	ENSP00000460269.1:n.1003C=
ENST00000576315.5:c.1036C=	ENSP00000460551.1:n.1036C=
ENST00000621655.1:c.1768C=	ENSP00000481436.1:n.1768C=
NM_000243.2:c.2231C= , LRG_190t1:c.2231C=	NP_000234.1:p.Ala744=
NM_001198536.1:c.*435C=	NP_001185465.1:n.*435C=
XM_017023236.2:c.2228C=	XP_016878725.1:p.Ala743=
NM_000243.3:c.2231C= MANE Select	NP_000234.1:p.Ala744=
NM_001198536.2:c.*435C=	NP_001185465.2:n.*435C=