Canonical Allele Identifier: CA394488964

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293887C>T (hg19) ; chr16:g.3243887C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243887C>T , CM000678.2:g.3243887C>T	GRCh38
NC_000016.9:g.3293887C>T , CM000678.1:g.3293887C>T	GRCh37
NC_000016.8:g.3233888C>T	NCBI36
NG_007871.1:g.17741G>A , LRG_190:g.17741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.886G>A
ENST00000219596.6:c.1765G>A MANE Select	ENSP00000219596.1:p.Glu589Lys
ENST00000219596.5:c.1765G>A	ENSP00000219596.1:p.Glu589Lys
ENST00000339854.8:c.1225G>A	ENSP00000339639.4:p.Glu409Lys
ENST00000536379.5:c.1132G>A	ENSP00000445079.1:p.Glu378Lys
ENST00000536980.5:c.*41G>A	ENSP00000444178.1:n.*41G>A
ENST00000537682.5:c.*41G>A	ENSP00000438611.1:n.*41G>A
ENST00000538326.5:c.*390G>A	ENSP00000437486.1:n.*390G>A
ENST00000539145.5:c.686G>A	ENSP00000444471.1:n.686G>A
ENST00000541159.5:c.1307G>A	ENSP00000438711.1:p.Gly436Glu
ENST00000542898.5:c.*41G>A	ENSP00000444615.1:n.*41G>A
ENST00000570511.5:c.1170G>A	ENSP00000458312.1:n.1170G>A
ENST00000572244.5:c.455G>A	ENSP00000461186.1:n.455G>A
ENST00000574583.5:c.537G>A	ENSP00000460269.1:n.537G>A
ENST00000576315.5:c.570G>A	ENSP00000460551.1:n.570G>A
ENST00000621655.1:c.1302G>A	ENSP00000481436.1:n.1302G>A
NM_000243.2:c.1765G>A , LRG_190t1:c.1765G>A	NP_000234.1:p.Glu589Lys
NM_001198536.1:c.1307G>A	NP_001185465.1:p.Arg436Lys
XM_017023236.2:c.1762G>A	XP_016878725.1:p.Glu588Lys
XR_001751903.1:n.2072G>A
NM_000243.3:c.1765G>A MANE Select	NP_000234.1:p.Glu589Lys
NM_001198536.2:c.1307G>A	NP_001185465.2:p.Gly436Glu