Canonical Allele Identifier: CA2202658566

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243262G= , CM000678.2:g.3243262G=	GRCh38
NC_000016.9:g.3293262G= , CM000678.1:g.3293262G=	GRCh37
NC_000016.8:g.3233263G=	NCBI36
NG_007871.1:g.18366C= , LRG_190:g.18366C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1346C=
ENST00000219596.6:c.2225C= MANE Select	ENSP00000219596.1:p.Thr742=
ENST00000219596.5:c.2225C=	ENSP00000219596.1:p.Thr742=
ENST00000339854.8:c.1685C=	ENSP00000339639.4:p.Thr562=
ENST00000536379.5:c.1592C=	ENSP00000445079.1:p.Thr531=
ENST00000536980.5:c.*501C=	ENSP00000444178.1:n.*501C=
ENST00000537682.5:c.*501C=	ENSP00000438611.1:n.*501C=
ENST00000538326.5:c.*850C=	ENSP00000437486.1:n.*850C=
ENST00000539145.5:c.1146C=	ENSP00000444471.1:n.1146C=
ENST00000541159.5:c.1767C=	ENSP00000438711.1:n.1767C=
ENST00000542898.5:c.*501C=	ENSP00000444615.1:n.*501C=
ENST00000570511.5:c.1630C=	ENSP00000458312.1:n.1630C=
ENST00000572244.5:c.915C=	ENSP00000461186.1:n.915C=
ENST00000574583.5:c.997C=	ENSP00000460269.1:n.997C=
ENST00000576315.5:c.1030C=	ENSP00000460551.1:n.1030C=
ENST00000621655.1:c.1762C=	ENSP00000481436.1:n.1762C=
NM_000243.2:c.2225C= , LRG_190t1:c.2225C=	NP_000234.1:p.Thr742=
NM_001198536.1:c.*429C=	NP_001185465.1:n.*429C=
XM_017023236.2:c.2222C=	XP_016878725.1:p.Thr741=
NM_000243.3:c.2225C= MANE Select	NP_000234.1:p.Thr742=
NM_001198536.2:c.*429C=	NP_001185465.2:n.*429C=