Canonical Allele Identifier: CA394486061

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293400T>C (hg19) ; chr16:g.3243400T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243400T>C , CM000678.2:g.3243400T>C	GRCh38
NC_000016.9:g.3293400T>C , CM000678.1:g.3293400T>C	GRCh37
NC_000016.8:g.3233401T>C	NCBI36
NG_007871.1:g.18228A>G , LRG_190:g.18228A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1208A>G
ENST00000219596.6:c.2087A>G MANE Select	ENSP00000219596.1:p.Glu696Gly
ENST00000219596.5:c.2087A>G	ENSP00000219596.1:p.Glu696Gly
ENST00000339854.8:c.1547A>G	ENSP00000339639.4:p.Glu516Gly
ENST00000536379.5:c.1454A>G	ENSP00000445079.1:p.Glu485Gly
ENST00000536980.5:c.*363A>G	ENSP00000444178.1:n.*363A>G
ENST00000537682.5:c.*363A>G	ENSP00000438611.1:n.*363A>G
ENST00000538326.5:c.*712A>G	ENSP00000437486.1:n.*712A>G
ENST00000539145.5:c.1008A>G	ENSP00000444471.1:n.1008A>G
ENST00000541159.5:c.1629A>G	ENSP00000438711.1:n.1629A>G
ENST00000542898.5:c.*363A>G	ENSP00000444615.1:n.*363A>G
ENST00000570511.5:c.1492A>G	ENSP00000458312.1:n.1492A>G
ENST00000572244.5:c.777A>G	ENSP00000461186.1:n.777A>G
ENST00000574583.5:c.859A>G	ENSP00000460269.1:n.859A>G
ENST00000576315.5:c.892A>G	ENSP00000460551.1:n.892A>G
ENST00000621655.1:c.1624A>G	ENSP00000481436.1:n.1624A>G
NM_000243.2:c.2087A>G , LRG_190t1:c.2087A>G	NP_000234.1:p.Glu696Gly
NM_001198536.1:c.*291A>G	NP_001185465.1:n.*291A>G
XM_017023236.2:c.2084A>G	XP_016878725.1:p.Glu695Gly
NM_000243.3:c.2087A>G MANE Select	NP_000234.1:p.Glu696Gly
NM_001198536.2:c.*291A>G	NP_001185465.2:n.*291A>G