Canonical Allele Identifier: CA394457785

Gene: MEFV

Linked Data

• gnomAD v4: 16-3244478-A-T
• MyVariant Identifiers: chr16:g.3294478A>T (hg19) ; chr16:g.3244478A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244478A>T , CM000678.2:g.3244478A>T	GRCh38
NC_000016.9:g.3294478A>T , CM000678.1:g.3294478A>T	GRCh37
NC_000016.8:g.3234479A>T	NCBI36
NG_007871.1:g.17150T>A , LRG_190:g.17150T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.842T>A
ENST00000219596.6:c.1721T>A MANE Select	ENSP00000219596.1:p.Phe574Tyr
ENST00000219596.5:c.1721T>A	ENSP00000219596.1:p.Phe574Tyr
ENST00000339854.8:c.1181T>A	ENSP00000339639.4:p.Phe394Tyr
ENST00000536379.5:c.1088T>A	ENSP00000445079.1:p.Phe363Tyr
ENST00000536980.5:c.1088T>A	ENSP00000444178.1:p.Phe363Tyr
ENST00000537682.5:c.1721T>A	ENSP00000438611.1:p.Phe574Tyr
ENST00000538326.5:c.*346T>A	ENSP00000437486.1:n.*346T>A
ENST00000539145.5:c.642T>A	ENSP00000444471.1:n.642T>A
ENST00000541159.5:c.1088T>A	ENSP00000438711.1:p.Phe363Tyr
ENST00000542898.5:c.1814T>A	ENSP00000444615.1:p.Phe605Tyr
ENST00000570511.5:c.1165-586T>A	ENSP00000458312.1:n.1165-586T>A
ENST00000572244.5:c.411T>A	ENSP00000461186.1:n.411T>A
ENST00000574583.5:c.532-586T>A	ENSP00000460269.1:n.532-586T>A
ENST00000576315.5:c.532-192T>A	ENSP00000460551.1:n.532-192T>A
ENST00000621655.1:c.1088T>A	ENSP00000481436.1:p.Phe363Tyr
NM_000243.2:c.1721T>A , LRG_190t1:c.1721T>A	NP_000234.1:p.Phe574Tyr
NM_001198536.1:c.1088T>A	NP_001185465.1:p.Phe363Tyr
XM_017023236.2:c.1718T>A	XP_016878725.1:p.Phe573Tyr
XR_001751903.1:n.1910T>A
NM_000243.3:c.1721T>A MANE Select	NP_000234.1:p.Phe574Tyr
NM_001198536.2:c.1088T>A	NP_001185465.2:p.Phe363Tyr