Canonical Allele Identifier: CA7860240

Gene: MEFV

Linked Data

• ClinVar Variation Id: 234501
• ClinVar RCV Id: RCV000214481 ; RCV001833230 ; RCV002478820 ; RCV003126635 ; RCV003126636
• dbSNP Id: rs377754606
• ExAC: 16:3299625 G / C
• gnomAD v2: 16-3299625-G-C
• gnomAD v3: 16-3249625-G-C
• gnomAD v4: 16-3249625-G-C
• MyVariant Identifiers: chr16:g.3299625G>C (hg19) ; chr16:g.3249625G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3249625G>C , CM000678.2:g.3249625G>C	GRCh38
NC_000016.9:g.3299625G>C , CM000678.1:g.3299625G>C	GRCh37
NC_000016.8:g.3239626G>C	NCBI36
NG_007871.1:g.12003C>G , LRG_190:g.12003C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.1066C>G MANE Select	ENSP00000219596.1:p.Gln356Glu
ENST00000219596.5:c.1066C>G	ENSP00000219596.1:p.Gln356Glu
ENST00000339854.8:c.526C>G	ENSP00000339639.4:p.Gln176Glu
ENST00000536379.5:c.433C>G	ENSP00000445079.1:p.Gln145Glu
ENST00000536980.5:c.433C>G	ENSP00000444178.1:p.Gln145Glu
ENST00000537682.5:c.1066C>G	ENSP00000438611.1:p.Gln356Glu
ENST00000538326.5:c.1066C>G	ENSP00000437486.1:p.Gln356Glu
ENST00000539145.5:c.278-2379C>G	ENSP00000444471.1:n.278-2379C>G
ENST00000541159.5:c.433C>G	ENSP00000438711.1:p.Gln145Glu
ENST00000542898.5:c.1159C>G	ENSP00000444615.1:p.Gln387Glu
ENST00000570511.5:c.911-2379C>G	ENSP00000458312.1:n.911-2379C>G
ENST00000572244.5:c.278-3078C>G	ENSP00000461186.1:n.278-3078C>G
ENST00000574583.5:c.278-2379C>G	ENSP00000460269.1:n.278-2379C>G
ENST00000576315.5:c.278-2379C>G	ENSP00000460551.1:n.278-2379C>G
ENST00000621655.1:c.433C>G	ENSP00000481436.1:p.Gln145Glu
NM_000243.2:c.1066C>G , LRG_190t1:c.1066C>G	NP_000234.1:p.Gln356Glu
NM_001198536.1:c.433C>G	NP_001185465.1:p.Gln145Glu
XM_017023236.2:c.1066C>G	XP_016878725.1:p.Gln356Glu
XR_001751903.1:n.1255C>G
NM_000243.3:c.1066C>G MANE Select	NP_000234.1:p.Gln356Glu
NM_001198536.2:c.433C>G	NP_001185465.2:p.Gln145Glu