Canonical Allele Identifier: CA394486972

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293481G>T (hg19) ; chr16:g.3243481G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243481G>T , CM000678.2:g.3243481G>T	GRCh38
NC_000016.9:g.3293481G>T , CM000678.1:g.3293481G>T	GRCh37
NC_000016.8:g.3233482G>T	NCBI36
NG_007871.1:g.18147C>A , LRG_190:g.18147C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1127C>A
ENST00000219596.6:c.2006C>A MANE Select	ENSP00000219596.1:p.Ala669Asp
ENST00000219596.5:c.2006C>A	ENSP00000219596.1:p.Ala669Asp
ENST00000339854.8:c.1466C>A	ENSP00000339639.4:p.Ala489Asp
ENST00000536379.5:c.1373C>A	ENSP00000445079.1:p.Ala458Asp
ENST00000536980.5:c.*282C>A	ENSP00000444178.1:n.*282C>A
ENST00000537682.5:c.*282C>A	ENSP00000438611.1:n.*282C>A
ENST00000538326.5:c.*631C>A	ENSP00000437486.1:n.*631C>A
ENST00000539145.5:c.927C>A	ENSP00000444471.1:n.927C>A
ENST00000541159.5:c.1548C>A	ENSP00000438711.1:n.1548C>A
ENST00000542898.5:c.*282C>A	ENSP00000444615.1:n.*282C>A
ENST00000570511.5:c.1411C>A	ENSP00000458312.1:n.1411C>A
ENST00000572244.5:c.696C>A	ENSP00000461186.1:n.696C>A
ENST00000574583.5:c.778C>A	ENSP00000460269.1:n.778C>A
ENST00000576315.5:c.811C>A	ENSP00000460551.1:n.811C>A
ENST00000621655.1:c.1543C>A	ENSP00000481436.1:n.1543C>A
NM_000243.2:c.2006C>A , LRG_190t1:c.2006C>A	NP_000234.1:p.Ala669Asp
NM_001198536.1:c.*210C>A	NP_001185465.1:n.*210C>A
XM_017023236.2:c.2003C>A	XP_016878725.1:p.Ala668Asp
NM_000243.3:c.2006C>A MANE Select	NP_000234.1:p.Ala669Asp
NM_001198536.2:c.*210C>A	NP_001185465.2:n.*210C>A