Canonical Allele Identifier: CA2202660591

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247078G= , CM000678.2:g.3247078G=	GRCh38
NC_000016.9:g.3297078G= , CM000678.1:g.3297078G=	GRCh37
NC_000016.8:g.3237079G=	NCBI36
NG_007871.1:g.14550C= , LRG_190:g.14550C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000219596.6:c.1525C= MANE Select	ENSP00000219596.1:p.Leu509=
ENST00000219596.5:c.1525C=	ENSP00000219596.1:p.Leu509=
ENST00000339854.8:c.985C=	ENSP00000339639.4:p.Leu329=
ENST00000536379.5:c.892C=	ENSP00000445079.1:p.Leu298=
ENST00000536980.5:c.892C=	ENSP00000444178.1:p.Leu298=
ENST00000537682.5:c.1525C=	ENSP00000438611.1:p.Leu509=
ENST00000538326.5:c.*150C=	ENSP00000437486.1:n.*150C=
ENST00000539145.5:c.446C=	ENSP00000444471.1:n.446C=
ENST00000539154.1:n.890C=
ENST00000541159.5:c.892C=	ENSP00000438711.1:p.Leu298=
ENST00000542898.5:c.1618C=	ENSP00000444615.1:p.Leu540=
ENST00000570511.5:c.1079C=	ENSP00000458312.1:n.1079C=
ENST00000572244.5:c.278-531C=	ENSP00000461186.1:n.278-531C=
ENST00000574583.5:c.446C=	ENSP00000460269.1:n.446C=
ENST00000576315.5:c.446C=	ENSP00000460551.1:n.446C=
ENST00000621655.1:c.892C=	ENSP00000481436.1:p.Leu298=
NM_000243.2:c.1525C= , LRG_190t1:c.1525C=	NP_000234.1:p.Leu509=
NM_001198536.1:c.892C=	NP_001185465.1:p.Leu298=
XM_017023236.2:c.1522C=	XP_016878725.1:p.Leu508=
XR_001751903.1:n.1714C=
NM_000243.3:c.1525C= MANE Select	NP_000234.1:p.Leu509=
NM_001198536.2:c.892C=	NP_001185465.2:p.Leu298=