Canonical Allele Identifier: CA2202659222

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244492C= , CM000678.2:g.3244492C=	GRCh38
NC_000016.9:g.3294492C= , CM000678.1:g.3294492C=	GRCh37
NC_000016.8:g.3234493C=	NCBI36
NG_007871.1:g.17136G= , LRG_190:g.17136G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.828G=
ENST00000219596.6:c.1707G= MANE Select	ENSP00000219596.1:p.Lys569=
ENST00000219596.5:c.1707G=	ENSP00000219596.1:p.Lys569=
ENST00000339854.8:c.1167G=	ENSP00000339639.4:p.Lys389=
ENST00000536379.5:c.1074G=	ENSP00000445079.1:p.Lys358=
ENST00000536980.5:c.1074G=	ENSP00000444178.1:p.Lys358=
ENST00000537682.5:c.1707G=	ENSP00000438611.1:p.Lys569=
ENST00000538326.5:c.*332G=	ENSP00000437486.1:n.*332G=
ENST00000539145.5:c.628G=	ENSP00000444471.1:n.628G=
ENST00000541159.5:c.1074G=	ENSP00000438711.1:p.Lys358=
ENST00000542898.5:c.1800G=	ENSP00000444615.1:p.Lys600=
ENST00000570511.5:c.1165-600G=	ENSP00000458312.1:n.1165-600G=
ENST00000572244.5:c.397G=	ENSP00000461186.1:n.397G=
ENST00000574583.5:c.532-600G=	ENSP00000460269.1:n.532-600G=
ENST00000576315.5:c.532-206G=	ENSP00000460551.1:n.532-206G=
ENST00000621655.1:c.1074G=	ENSP00000481436.1:p.Lys358=
NM_000243.2:c.1707G= , LRG_190t1:c.1707G=	NP_000234.1:p.Lys569=
NM_001198536.1:c.1074G=	NP_001185465.1:p.Lys358=
XM_017023236.2:c.1704G=	XP_016878725.1:p.Lys568=
XR_001751903.1:n.1896G=
NM_000243.3:c.1707G= MANE Select	NP_000234.1:p.Lys569=
NM_001198536.2:c.1074G=	NP_001185465.2:p.Lys358=