Canonical Allele Identifier: CA394485623

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293325A>T (hg19) ; chr16:g.3243325A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243325A>T , CM000678.2:g.3243325A>T	GRCh38
NC_000016.9:g.3293325A>T , CM000678.1:g.3293325A>T	GRCh37
NC_000016.8:g.3233326A>T	NCBI36
NG_007871.1:g.18303T>A , LRG_190:g.18303T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1283T>A
ENST00000219596.6:c.2162T>A MANE Select	ENSP00000219596.1:p.Phe721Tyr
ENST00000219596.5:c.2162T>A	ENSP00000219596.1:p.Phe721Tyr
ENST00000339854.8:c.1622T>A	ENSP00000339639.4:p.Phe541Tyr
ENST00000536379.5:c.1529T>A	ENSP00000445079.1:p.Phe510Tyr
ENST00000536980.5:c.*438T>A	ENSP00000444178.1:n.*438T>A
ENST00000537682.5:c.*438T>A	ENSP00000438611.1:n.*438T>A
ENST00000538326.5:c.*787T>A	ENSP00000437486.1:n.*787T>A
ENST00000539145.5:c.1083T>A	ENSP00000444471.1:n.1083T>A
ENST00000541159.5:c.1704T>A	ENSP00000438711.1:n.1704T>A
ENST00000542898.5:c.*438T>A	ENSP00000444615.1:n.*438T>A
ENST00000570511.5:c.1567T>A	ENSP00000458312.1:n.1567T>A
ENST00000572244.5:c.852T>A	ENSP00000461186.1:n.852T>A
ENST00000574583.5:c.934T>A	ENSP00000460269.1:n.934T>A
ENST00000576315.5:c.967T>A	ENSP00000460551.1:n.967T>A
ENST00000621655.1:c.1699T>A	ENSP00000481436.1:n.1699T>A
NM_000243.2:c.2162T>A , LRG_190t1:c.2162T>A	NP_000234.1:p.Phe721Tyr
NM_001198536.1:c.*366T>A	NP_001185465.1:n.*366T>A
XM_017023236.2:c.2159T>A	XP_016878725.1:p.Phe720Tyr
NM_000243.3:c.2162T>A MANE Select	NP_000234.1:p.Phe721Tyr
NM_001198536.2:c.*366T>A	NP_001185465.2:n.*366T>A