Canonical Allele Identifier: CA394465166

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247235T>G , CM000678.2:g.3247235T>G	GRCh38
NC_000016.9:g.3297235T>G , CM000678.1:g.3297235T>G	GRCh37
NC_000016.8:g.3237236T>G	NCBI36
NG_007871.1:g.14393A>C , LRG_190:g.14393A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000243.3:c.1368A>C MANE Select	NP_000234.1:p.Glu456Asp
ENST00000219596.6:c.1368A>C MANE Select	ENSP00000219596.1:p.Glu456Asp
NM_000243.2:c.1368A>C , LRG_190t1:c.1368A>C	NP_000234.1:p.Glu456Asp
NM_001198536.1:c.735A>C	NP_001185465.1:p.Glu245Asp
NM_001198536.2:c.735A>C	NP_001185465.2:p.Glu245Asp
ENST00000219596.5:c.1368A>C	ENSP00000219596.1:p.Glu456Asp
ENST00000339854.8:c.828A>C	ENSP00000339639.4:p.Glu276Asp
ENST00000536379.5:c.735A>C	ENSP00000445079.1:p.Glu245Asp
ENST00000536980.5:c.735A>C	ENSP00000444178.1:p.Glu245Asp
ENST00000537682.5:c.1368A>C	ENSP00000438611.1:p.Glu456Asp
ENST00000538326.5:c.1466A>C	ENSP00000437486.1:p.Lys489Thr
ENST00000539145.5:c.289A>C	ENSP00000444471.1:n.289A>C
ENST00000539154.1:n.733A>C
ENST00000541159.5:c.735A>C	ENSP00000438711.1:p.Glu245Asp
ENST00000542898.5:c.1461A>C	ENSP00000444615.1:p.Glu487Asp
ENST00000570511.5:c.922A>C	ENSP00000458312.1:n.922A>C
ENST00000572244.5:c.278-688A>C	ENSP00000461186.1:n.278-688A>C
ENST00000574583.5:c.289A>C	ENSP00000460269.1:n.289A>C
ENST00000576315.5:c.289A>C	ENSP00000460551.1:n.289A>C
ENST00000621655.1:c.735A>C	ENSP00000481436.1:p.Glu245Asp
XM_017023236.2:c.1365A>C	XP_016878725.1:p.Glu455Asp
XR_001751903.1:n.1557A>C