Canonical Allele Identifier: CA276955088

Gene: MEFV

Linked Data

• ClinVar Variation Id: 649340
• ClinVar RCV Id: RCV000804253 ; RCV001274311 ; RCV002487716 ; RCV003127470 ; RCV003479222
• dbSNP Id: rs200375017
• gnomAD v2: 16-3293364-C-T
• gnomAD v3: 16-3243364-C-T
• gnomAD v4: 16-3243364-C-T
• MyVariant Identifiers: chr16:g.3293364C>T (hg19) ; chr16:g.3243364C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243364C>T , CM000678.2:g.3243364C>T	GRCh38
NC_000016.9:g.3293364C>T , CM000678.1:g.3293364C>T	GRCh37
NC_000016.8:g.3233365C>T	NCBI36
NG_007871.1:g.18264G>A , LRG_190:g.18264G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1244G>A
ENST00000219596.6:c.2123G>A MANE Select	ENSP00000219596.1:p.Arg708His
ENST00000219596.5:c.2123G>A	ENSP00000219596.1:p.Arg708His
ENST00000339854.8:c.1583G>A	ENSP00000339639.4:p.Arg528His
ENST00000536379.5:c.1490G>A	ENSP00000445079.1:p.Arg497His
ENST00000536980.5:c.*399G>A	ENSP00000444178.1:n.*399G>A
ENST00000537682.5:c.*399G>A	ENSP00000438611.1:n.*399G>A
ENST00000538326.5:c.*748G>A	ENSP00000437486.1:n.*748G>A
ENST00000539145.5:c.1044G>A	ENSP00000444471.1:n.1044G>A
ENST00000541159.5:c.1665G>A	ENSP00000438711.1:n.1665G>A
ENST00000542898.5:c.*399G>A	ENSP00000444615.1:n.*399G>A
ENST00000570511.5:c.1528G>A	ENSP00000458312.1:n.1528G>A
ENST00000572244.5:c.813G>A	ENSP00000461186.1:n.813G>A
ENST00000574583.5:c.895G>A	ENSP00000460269.1:n.895G>A
ENST00000576315.5:c.928G>A	ENSP00000460551.1:n.928G>A
ENST00000621655.1:c.1660G>A	ENSP00000481436.1:n.1660G>A
NM_000243.2:c.2123G>A , LRG_190t1:c.2123G>A	NP_000234.1:p.Arg708His
NM_001198536.1:c.*327G>A	NP_001185465.1:n.*327G>A
XM_017023236.2:c.2120G>A	XP_016878725.1:p.Arg707His
NM_000243.3:c.2123G>A MANE Select	NP_000234.1:p.Arg708His
NM_001198536.2:c.*327G>A	NP_001185465.2:n.*327G>A