Canonical Allele Identifier: CA2202658581

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243286A= , CM000678.2:g.3243286A=	GRCh38
NC_000016.9:g.3293286A= , CM000678.1:g.3293286A=	GRCh37
NC_000016.8:g.3233287A=	NCBI36
NG_007871.1:g.18342T= , LRG_190:g.18342T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1322T=
ENST00000219596.6:c.2201T= MANE Select	ENSP00000219596.1:p.Val734=
ENST00000219596.5:c.2201T=	ENSP00000219596.1:p.Val734=
ENST00000339854.8:c.1661T=	ENSP00000339639.4:p.Val554=
ENST00000536379.5:c.1568T=	ENSP00000445079.1:p.Val523=
ENST00000536980.5:c.*477T=	ENSP00000444178.1:n.*477T=
ENST00000537682.5:c.*477T=	ENSP00000438611.1:n.*477T=
ENST00000538326.5:c.*826T=	ENSP00000437486.1:n.*826T=
ENST00000539145.5:c.1122T=	ENSP00000444471.1:n.1122T=
ENST00000541159.5:c.1743T=	ENSP00000438711.1:n.1743T=
ENST00000542898.5:c.*477T=	ENSP00000444615.1:n.*477T=
ENST00000570511.5:c.1606T=	ENSP00000458312.1:n.1606T=
ENST00000572244.5:c.891T=	ENSP00000461186.1:n.891T=
ENST00000574583.5:c.973T=	ENSP00000460269.1:n.973T=
ENST00000576315.5:c.1006T=	ENSP00000460551.1:n.1006T=
ENST00000621655.1:c.1738T=	ENSP00000481436.1:n.1738T=
NM_000243.2:c.2201T= , LRG_190t1:c.2201T=	NP_000234.1:p.Val734=
NM_001198536.1:c.*405T=	NP_001185465.1:n.*405T=
XM_017023236.2:c.2198T=	XP_016878725.1:p.Val733=
NM_000243.3:c.2201T= MANE Select	NP_000234.1:p.Val734=
NM_001198536.2:c.*405T=	NP_001185465.2:n.*405T=