Canonical Allele Identifier: CA2202659078

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244187A= , CM000678.2:g.3244187A=	GRCh38
NC_000016.9:g.3294187A= , CM000678.1:g.3294187A=	GRCh37
NC_000016.8:g.3234188A=	NCBI36
NG_007871.1:g.17441T= , LRG_190:g.17441T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.880+67T=
ENST00000219596.6:c.1759+67T= MANE Select	ENSP00000219596.1:n.1759+67T=
ENST00000219596.5:c.1759+67T=	ENSP00000219596.1:n.1759+67T=
ENST00000339854.8:c.1219+67T=	ENSP00000339639.4:n.1219+67T=
ENST00000536379.5:c.1126+67T=	ENSP00000445079.1:n.1126+67T=
ENST00000536980.5:c.1193T=	ENSP00000444178.1:p.Leu398=
ENST00000537682.5:c.1826T=	ENSP00000438611.1:p.Leu609=
ENST00000538326.5:c.*384+67T=	ENSP00000437486.1:n.*384+67T=
ENST00000539145.5:c.680+67T=	ENSP00000444471.1:n.680+67T=
ENST00000541159.5:c.1126+67T=	ENSP00000438711.1:n.1126+67T=
ENST00000542898.5:c.1919T=	ENSP00000444615.1:p.Leu640=
ENST00000570511.5:c.1165-295T=	ENSP00000458312.1:n.1165-295T=
ENST00000572244.5:c.449+67T=	ENSP00000461186.1:n.449+67T=
ENST00000574583.5:c.532-295T=	ENSP00000460269.1:n.532-295T=
ENST00000576315.5:c.564+67T=	ENSP00000460551.1:n.564+67T=
ENST00000621655.1:c.1126+67T=	ENSP00000481436.1:n.1126+67T=
NM_000243.2:c.1759+67T= , LRG_190t1:c.1759+67T=	NP_000234.1:n.1759+67T=
NM_001198536.1:c.1126+67T=	NP_001185465.1:n.1126+67T=
XM_017023236.2:c.1756+67T=	XP_016878725.1:n.1756+67T=
XR_001751903.1:n.2015T=
NM_000243.3:c.1759+67T= MANE Select	NP_000234.1:n.1759+67T=
NM_001198536.2:c.1126+67T=	NP_001185465.2:n.1126+67T=