Canonical Allele Identifier: CA280491

Gene: MEFV

Linked Data

• ClinVar Variation Id: 97481
• ClinVar RCV Id: RCV000083733
• dbSNP Id: rs104895090
• MyVariant Identifiers: chr16:g.3293445G>A (hg19) ; chr16:g.3243445G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243445G>A , CM000678.2:g.3243445G>A	GRCh38
NC_000016.9:g.3293445G>A , CM000678.1:g.3293445G>A	GRCh37
NC_000016.8:g.3233446G>A	NCBI36
NG_007871.1:g.18183C>T , LRG_190:g.18183C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1163C>T
ENST00000219596.6:c.2042C>T MANE Select	ENSP00000219596.1:p.Thr681Ile
ENST00000219596.5:c.2042C>T	ENSP00000219596.1:p.Thr681Ile
ENST00000339854.8:c.1502C>T	ENSP00000339639.4:p.Thr501Ile
ENST00000536379.5:c.1409C>T	ENSP00000445079.1:p.Thr470Ile
ENST00000536980.5:c.*318C>T	ENSP00000444178.1:n.*318C>T
ENST00000537682.5:c.*318C>T	ENSP00000438611.1:n.*318C>T
ENST00000538326.5:c.*667C>T	ENSP00000437486.1:n.*667C>T
ENST00000539145.5:c.963C>T	ENSP00000444471.1:n.963C>T
ENST00000541159.5:c.1584C>T	ENSP00000438711.1:n.1584C>T
ENST00000542898.5:c.*318C>T	ENSP00000444615.1:n.*318C>T
ENST00000570511.5:c.1447C>T	ENSP00000458312.1:n.1447C>T
ENST00000572244.5:c.732C>T	ENSP00000461186.1:n.732C>T
ENST00000574583.5:c.814C>T	ENSP00000460269.1:n.814C>T
ENST00000576315.5:c.847C>T	ENSP00000460551.1:n.847C>T
ENST00000621655.1:c.1579C>T	ENSP00000481436.1:n.1579C>T
NM_000243.2:c.2042C>T , LRG_190t1:c.2042C>T	NP_000234.1:p.Thr681Ile
NM_001198536.1:c.*246C>T	NP_001185465.1:n.*246C>T
XM_017023236.2:c.2039C>T	XP_016878725.1:p.Thr680Ile
NM_000243.3:c.2042C>T MANE Select	NP_000234.1:p.Thr681Ile
NM_001198536.2:c.*246C>T	NP_001185465.2:n.*246C>T