Canonical Allele Identifier: CA2202658565

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243261T= , CM000678.2:g.3243261T=	GRCh38
NC_000016.9:g.3293261T= , CM000678.1:g.3293261T=	GRCh37
NC_000016.8:g.3233262T=	NCBI36
NG_007871.1:g.18367A= , LRG_190:g.18367A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1347A=
ENST00000219596.6:c.2226A= MANE Select	ENSP00000219596.1:p.Thr742=
ENST00000219596.5:c.2226A=	ENSP00000219596.1:p.Thr742=
ENST00000339854.8:c.1686A=	ENSP00000339639.4:p.Thr562=
ENST00000536379.5:c.1593A=	ENSP00000445079.1:p.Thr531=
ENST00000536980.5:c.*502A=	ENSP00000444178.1:n.*502A=
ENST00000537682.5:c.*502A=	ENSP00000438611.1:n.*502A=
ENST00000538326.5:c.*851A=	ENSP00000437486.1:n.*851A=
ENST00000539145.5:c.1147A=	ENSP00000444471.1:n.1147A=
ENST00000541159.5:c.1768A=	ENSP00000438711.1:n.1768A=
ENST00000542898.5:c.*502A=	ENSP00000444615.1:n.*502A=
ENST00000570511.5:c.1631A=	ENSP00000458312.1:n.1631A=
ENST00000572244.5:c.916A=	ENSP00000461186.1:n.916A=
ENST00000574583.5:c.998A=	ENSP00000460269.1:n.998A=
ENST00000576315.5:c.1031A=	ENSP00000460551.1:n.1031A=
ENST00000621655.1:c.1763A=	ENSP00000481436.1:n.1763A=
NM_000243.2:c.2226A= , LRG_190t1:c.2226A=	NP_000234.1:p.Thr742=
NM_001198536.1:c.*430A=	NP_001185465.1:n.*430A=
XM_017023236.2:c.2223A=	XP_016878725.1:p.Thr741=
NM_000243.3:c.2226A= MANE Select	NP_000234.1:p.Thr742=
NM_001198536.2:c.*430A=	NP_001185465.2:n.*430A=