Canonical Allele Identifier: CA2202659120

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244277C= , CM000678.2:g.3244277C=	GRCh38
NC_000016.9:g.3294277C= , CM000678.1:g.3294277C=	GRCh37
NC_000016.8:g.3234278C=	NCBI36
NG_007871.1:g.17351G= , LRG_190:g.17351G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.857G=
ENST00000219596.6:c.1736G= MANE Select	ENSP00000219596.1:p.Arg579=
ENST00000219596.5:c.1736G=	ENSP00000219596.1:p.Arg579=
ENST00000339854.8:c.1196G=	ENSP00000339639.4:p.Arg399=
ENST00000536379.5:c.1103G=	ENSP00000445079.1:p.Arg368=
ENST00000536980.5:c.1103G=	ENSP00000444178.1:p.Arg368=
ENST00000537682.5:c.1736G=	ENSP00000438611.1:p.Arg579=
ENST00000538326.5:c.*361G=	ENSP00000437486.1:n.*361G=
ENST00000539145.5:c.657G=	ENSP00000444471.1:n.657G=
ENST00000541159.5:c.1103G=	ENSP00000438711.1:p.Arg368=
ENST00000542898.5:c.1829G=	ENSP00000444615.1:p.Arg610=
ENST00000570511.5:c.1165-385G=	ENSP00000458312.1:n.1165-385G=
ENST00000572244.5:c.426G=	ENSP00000461186.1:n.426G=
ENST00000574583.5:c.532-385G=	ENSP00000460269.1:n.532-385G=
ENST00000576315.5:c.541G=	ENSP00000460551.1:n.541G=
ENST00000621655.1:c.1103G=	ENSP00000481436.1:p.Arg368=
NM_000243.2:c.1736G= , LRG_190t1:c.1736G=	NP_000234.1:p.Arg579=
NM_001198536.1:c.1103G=	NP_001185465.1:p.Arg368=
XM_017023236.2:c.1733G=	XP_016878725.1:p.Arg578=
XR_001751903.1:n.1925G=
NM_000243.3:c.1736G= MANE Select	NP_000234.1:p.Arg579=
NM_001198536.2:c.1103G=	NP_001185465.2:p.Arg368=