Canonical Allele Identifier: CA2202659080

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244194C= , CM000678.2:g.3244194C=	GRCh38
NC_000016.9:g.3294194C= , CM000678.1:g.3294194C=	GRCh37
NC_000016.8:g.3234195C=	NCBI36
NG_007871.1:g.17434G= , LRG_190:g.17434G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.880+60G=
ENST00000219596.6:c.1759+60G= MANE Select	ENSP00000219596.1:n.1759+60G=
ENST00000219596.5:c.1759+60G=	ENSP00000219596.1:n.1759+60G=
ENST00000339854.8:c.1219+60G=	ENSP00000339639.4:n.1219+60G=
ENST00000536379.5:c.1126+60G=	ENSP00000445079.1:n.1126+60G=
ENST00000536980.5:c.1186G=	ENSP00000444178.1:p.Val396=
ENST00000537682.5:c.1819G=	ENSP00000438611.1:p.Val607=
ENST00000538326.5:c.*384+60G=	ENSP00000437486.1:n.*384+60G=
ENST00000539145.5:c.680+60G=	ENSP00000444471.1:n.680+60G=
ENST00000541159.5:c.1126+60G=	ENSP00000438711.1:n.1126+60G=
ENST00000542898.5:c.1912G=	ENSP00000444615.1:p.Val638=
ENST00000570511.5:c.1165-302G=	ENSP00000458312.1:n.1165-302G=
ENST00000572244.5:c.449+60G=	ENSP00000461186.1:n.449+60G=
ENST00000574583.5:c.532-302G=	ENSP00000460269.1:n.532-302G=
ENST00000576315.5:c.564+60G=	ENSP00000460551.1:n.564+60G=
ENST00000621655.1:c.1126+60G=	ENSP00000481436.1:n.1126+60G=
NM_000243.2:c.1759+60G= , LRG_190t1:c.1759+60G=	NP_000234.1:n.1759+60G=
NM_001198536.1:c.1126+60G=	NP_001185465.1:n.1126+60G=
XM_017023236.2:c.1756+60G=	XP_016878725.1:n.1756+60G=
XR_001751903.1:n.2008G=
NM_000243.3:c.1759+60G= MANE Select	NP_000234.1:n.1759+60G=
NM_001198536.2:c.1126+60G=	NP_001185465.2:n.1126+60G=