Canonical Allele Identifier: CA2202659218

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244487G= , CM000678.2:g.3244487G=	GRCh38
NC_000016.9:g.3294487G= , CM000678.1:g.3294487G=	GRCh37
NC_000016.8:g.3234488G=	NCBI36
NG_007871.1:g.17141C= , LRG_190:g.17141C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.833C=
ENST00000219596.6:c.1712C= MANE Select	ENSP00000219596.1:p.Thr571=
ENST00000219596.5:c.1712C=	ENSP00000219596.1:p.Thr571=
ENST00000339854.8:c.1172C=	ENSP00000339639.4:p.Thr391=
ENST00000536379.5:c.1079C=	ENSP00000445079.1:p.Thr360=
ENST00000536980.5:c.1079C=	ENSP00000444178.1:p.Thr360=
ENST00000537682.5:c.1712C=	ENSP00000438611.1:p.Thr571=
ENST00000538326.5:c.*337C=	ENSP00000437486.1:n.*337C=
ENST00000539145.5:c.633C=	ENSP00000444471.1:n.633C=
ENST00000541159.5:c.1079C=	ENSP00000438711.1:p.Thr360=
ENST00000542898.5:c.1805C=	ENSP00000444615.1:p.Thr602=
ENST00000570511.5:c.1165-595C=	ENSP00000458312.1:n.1165-595C=
ENST00000572244.5:c.402C=	ENSP00000461186.1:n.402C=
ENST00000574583.5:c.532-595C=	ENSP00000460269.1:n.532-595C=
ENST00000576315.5:c.532-201C=	ENSP00000460551.1:n.532-201C=
ENST00000621655.1:c.1079C=	ENSP00000481436.1:p.Thr360=
NM_000243.2:c.1712C= , LRG_190t1:c.1712C=	NP_000234.1:p.Thr571=
NM_001198536.1:c.1079C=	NP_001185465.1:p.Thr360=
XM_017023236.2:c.1709C=	XP_016878725.1:p.Thr570=
XR_001751903.1:n.1901C=
NM_000243.3:c.1712C= MANE Select	NP_000234.1:p.Thr571=
NM_001198536.2:c.1079C=	NP_001185465.2:p.Thr360=