Canonical Allele Identifier: CA394486034

Gene: MEFV

Linked Data

• gnomAD v4: 16-3243395-C-A
• MyVariant Identifiers: chr16:g.3293395C>A (hg19) ; chr16:g.3243395C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243395C>A , CM000678.2:g.3243395C>A	GRCh38
NC_000016.9:g.3293395C>A , CM000678.1:g.3293395C>A	GRCh37
NC_000016.8:g.3233396C>A	NCBI36
NG_007871.1:g.18233G>T , LRG_190:g.18233G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1213G>T
ENST00000219596.6:c.2092G>T MANE Select	ENSP00000219596.1:p.Glu698Ter
ENST00000219596.5:c.2092G>T	ENSP00000219596.1:p.Glu698Ter
ENST00000339854.8:c.1552G>T	ENSP00000339639.4:p.Glu518Ter
ENST00000536379.5:c.1459G>T	ENSP00000445079.1:p.Glu487Ter
ENST00000536980.5:c.*368G>T	ENSP00000444178.1:n.*368G>T
ENST00000537682.5:c.*368G>T	ENSP00000438611.1:n.*368G>T
ENST00000538326.5:c.*717G>T	ENSP00000437486.1:n.*717G>T
ENST00000539145.5:c.1013G>T	ENSP00000444471.1:n.1013G>T
ENST00000541159.5:c.1634G>T	ENSP00000438711.1:n.1634G>T
ENST00000542898.5:c.*368G>T	ENSP00000444615.1:n.*368G>T
ENST00000570511.5:c.1497G>T	ENSP00000458312.1:n.1497G>T
ENST00000572244.5:c.782G>T	ENSP00000461186.1:n.782G>T
ENST00000574583.5:c.864G>T	ENSP00000460269.1:n.864G>T
ENST00000576315.5:c.897G>T	ENSP00000460551.1:n.897G>T
ENST00000621655.1:c.1629G>T	ENSP00000481436.1:n.1629G>T
NM_000243.2:c.2092G>T , LRG_190t1:c.2092G>T	NP_000234.1:p.Glu698Ter
NM_001198536.1:c.*296G>T	NP_001185465.1:n.*296G>T
XM_017023236.2:c.2089G>T	XP_016878725.1:p.Glu697Ter
NM_000243.3:c.2092G>T MANE Select	NP_000234.1:p.Glu698Ter
NM_001198536.2:c.*296G>T	NP_001185465.2:n.*296G>T