Canonical Allele Identifier: CA2202661929

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3249493G= , CM000678.2:g.3249493G=	GRCh38
NC_000016.9:g.3299493G= , CM000678.1:g.3299493G=	GRCh37
NC_000016.8:g.3239494G=	NCBI36
NG_007871.1:g.12135C= , LRG_190:g.12135C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000219596.6:c.1198C= MANE Select	ENSP00000219596.1:p.Leu400=
ENST00000219596.5:c.1198C=	ENSP00000219596.1:p.Leu400=
ENST00000339854.8:c.658C=	ENSP00000339639.4:p.Leu220=
ENST00000536379.5:c.565C=	ENSP00000445079.1:p.Leu189=
ENST00000536980.5:c.565C=	ENSP00000444178.1:p.Leu189=
ENST00000537682.5:c.1198C=	ENSP00000438611.1:p.Leu400=
ENST00000538326.5:c.1198C=	ENSP00000437486.1:p.Leu400=
ENST00000539145.5:c.278-2247C=	ENSP00000444471.1:n.278-2247C=
ENST00000541159.5:c.565C=	ENSP00000438711.1:p.Leu189=
ENST00000542898.5:c.1291C=	ENSP00000444615.1:p.Leu431=
ENST00000570511.5:c.911-2247C=	ENSP00000458312.1:n.911-2247C=
ENST00000572244.5:c.278-2946C=	ENSP00000461186.1:n.278-2946C=
ENST00000574583.5:c.278-2247C=	ENSP00000460269.1:n.278-2247C=
ENST00000576315.5:c.278-2247C=	ENSP00000460551.1:n.278-2247C=
ENST00000621655.1:c.565C=	ENSP00000481436.1:p.Leu189=
NM_000243.2:c.1198C= , LRG_190t1:c.1198C=	NP_000234.1:p.Leu400=
NM_001198536.1:c.565C=	NP_001185465.1:p.Leu189=
XM_017023236.2:c.1198C=	XP_016878725.1:p.Leu400=
XR_001751903.1:n.1387C=
NM_000243.3:c.1198C= MANE Select	NP_000234.1:p.Leu400=
NM_001198536.2:c.565C=	NP_001185465.2:p.Leu189=