Canonical Allele Identifier: CA2202659224

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244498C= , CM000678.2:g.3244498C=	GRCh38
NC_000016.9:g.3294498C= , CM000678.1:g.3294498C=	GRCh37
NC_000016.8:g.3234499C=	NCBI36
NG_007871.1:g.17130G= , LRG_190:g.17130G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.822G=
ENST00000219596.6:c.1701G= MANE Select	ENSP00000219596.1:p.Val567=
ENST00000219596.5:c.1701G=	ENSP00000219596.1:p.Val567=
ENST00000339854.8:c.1161G=	ENSP00000339639.4:p.Val387=
ENST00000536379.5:c.1068G=	ENSP00000445079.1:p.Val356=
ENST00000536980.5:c.1068G=	ENSP00000444178.1:p.Val356=
ENST00000537682.5:c.1701G=	ENSP00000438611.1:p.Val567=
ENST00000538326.5:c.*326G=	ENSP00000437486.1:n.*326G=
ENST00000539145.5:c.622G=	ENSP00000444471.1:n.622G=
ENST00000541159.5:c.1068G=	ENSP00000438711.1:p.Val356=
ENST00000542898.5:c.1794G=	ENSP00000444615.1:p.Val598=
ENST00000570511.5:c.1165-606G=	ENSP00000458312.1:n.1165-606G=
ENST00000572244.5:c.391G=	ENSP00000461186.1:n.391G=
ENST00000574583.5:c.532-606G=	ENSP00000460269.1:n.532-606G=
ENST00000576315.5:c.532-212G=	ENSP00000460551.1:n.532-212G=
ENST00000621655.1:c.1068G=	ENSP00000481436.1:p.Val356=
NM_000243.2:c.1701G= , LRG_190t1:c.1701G=	NP_000234.1:p.Val567=
NM_001198536.1:c.1068G=	NP_001185465.1:p.Val356=
XM_017023236.2:c.1698G=	XP_016878725.1:p.Val566=
XR_001751903.1:n.1890G=
NM_000243.3:c.1701G= MANE Select	NP_000234.1:p.Val567=
NM_001198536.2:c.1068G=	NP_001185465.2:p.Val356=