Canonical Allele Identifier: CA2202658632

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243378G= , CM000678.2:g.3243378G=	GRCh38
NC_000016.9:g.3293378G= , CM000678.1:g.3293378G=	GRCh37
NC_000016.8:g.3233379G=	NCBI36
NG_007871.1:g.18250C= , LRG_190:g.18250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1230C=
ENST00000219596.6:c.2109C= MANE Select	ENSP00000219596.1:p.Ser703=
ENST00000219596.5:c.2109C=	ENSP00000219596.1:p.Ser703=
ENST00000339854.8:c.1569C=	ENSP00000339639.4:p.Ser523=
ENST00000536379.5:c.1476C=	ENSP00000445079.1:p.Ser492=
ENST00000536980.5:c.*385C=	ENSP00000444178.1:n.*385C=
ENST00000537682.5:c.*385C=	ENSP00000438611.1:n.*385C=
ENST00000538326.5:c.*734C=	ENSP00000437486.1:n.*734C=
ENST00000539145.5:c.1030C=	ENSP00000444471.1:n.1030C=
ENST00000541159.5:c.1651C=	ENSP00000438711.1:n.1651C=
ENST00000542898.5:c.*385C=	ENSP00000444615.1:n.*385C=
ENST00000570511.5:c.1514C=	ENSP00000458312.1:n.1514C=
ENST00000572244.5:c.799C=	ENSP00000461186.1:n.799C=
ENST00000574583.5:c.881C=	ENSP00000460269.1:n.881C=
ENST00000576315.5:c.914C=	ENSP00000460551.1:n.914C=
ENST00000621655.1:c.1646C=	ENSP00000481436.1:n.1646C=
NM_000243.2:c.2109C= , LRG_190t1:c.2109C=	NP_000234.1:p.Ser703=
NM_001198536.1:c.*313C=	NP_001185465.1:n.*313C=
XM_017023236.2:c.2106C=	XP_016878725.1:p.Ser702=
NM_000243.3:c.2109C= MANE Select	NP_000234.1:p.Ser703=
NM_001198536.2:c.*313C=	NP_001185465.2:n.*313C=