Canonical Allele Identifier: CA276955032

Gene: MEFV

Linked Data

• ClinVar Variation Id: 1580755
• ClinVar RCV Id: RCV002085975
• dbSNP Id: rs956722067
• gnomAD v2: 16-3293285-C-T
• gnomAD v3: 16-3243285-C-T
• gnomAD v4: 16-3243285-C-T
• MyVariant Identifiers: chr16:g.3293285C>T (hg19) ; chr16:g.3243285C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243285C>T , CM000678.2:g.3243285C>T	GRCh38
NC_000016.9:g.3293285C>T , CM000678.1:g.3293285C>T	GRCh37
NC_000016.8:g.3233286C>T	NCBI36
NG_007871.1:g.18343G>A , LRG_190:g.18343G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1323G>A
ENST00000219596.6:c.2202G>A MANE Select	ENSP00000219596.1:p.Val734=
ENST00000219596.5:c.2202G>A	ENSP00000219596.1:p.Val734=
ENST00000339854.8:c.1662G>A	ENSP00000339639.4:p.Val554=
ENST00000536379.5:c.1569G>A	ENSP00000445079.1:p.Val523=
ENST00000536980.5:c.*478G>A	ENSP00000444178.1:n.*478G>A
ENST00000537682.5:c.*478G>A	ENSP00000438611.1:n.*478G>A
ENST00000538326.5:c.*827G>A	ENSP00000437486.1:n.*827G>A
ENST00000539145.5:c.1123G>A	ENSP00000444471.1:n.1123G>A
ENST00000541159.5:c.1744G>A	ENSP00000438711.1:n.1744G>A
ENST00000542898.5:c.*478G>A	ENSP00000444615.1:n.*478G>A
ENST00000570511.5:c.1607G>A	ENSP00000458312.1:n.1607G>A
ENST00000572244.5:c.892G>A	ENSP00000461186.1:n.892G>A
ENST00000574583.5:c.974G>A	ENSP00000460269.1:n.974G>A
ENST00000576315.5:c.1007G>A	ENSP00000460551.1:n.1007G>A
ENST00000621655.1:c.1739G>A	ENSP00000481436.1:n.1739G>A
NM_000243.2:c.2202G>A , LRG_190t1:c.2202G>A	NP_000234.1:p.Val734=
NM_001198536.1:c.*406G>A	NP_001185465.1:n.*406G>A
XM_017023236.2:c.2199G>A	XP_016878725.1:p.Val733=
NM_000243.3:c.2202G>A MANE Select	NP_000234.1:p.Val734=
NM_001198536.2:c.*406G>A	NP_001185465.2:n.*406G>A