Canonical Allele Identifier: CA394464657

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3297189A>G (hg19) ; chr16:g.3247189A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247189A>G , CM000678.2:g.3247189A>G	GRCh38
NC_000016.9:g.3297189A>G , CM000678.1:g.3297189A>G	GRCh37
NC_000016.8:g.3237190A>G	NCBI36
NG_007871.1:g.14439T>C , LRG_190:g.14439T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000219596.6:c.1414T>C MANE Select	ENSP00000219596.1:p.Phe472Leu
ENST00000219596.5:c.1414T>C	ENSP00000219596.1:p.Phe472Leu
ENST00000339854.8:c.874T>C	ENSP00000339639.4:p.Phe292Leu
ENST00000536379.5:c.781T>C	ENSP00000445079.1:p.Phe261Leu
ENST00000536980.5:c.781T>C	ENSP00000444178.1:p.Phe261Leu
ENST00000537682.5:c.1414T>C	ENSP00000438611.1:p.Phe472Leu
ENST00000538326.5:c.*39T>C	ENSP00000437486.1:n.*39T>C
ENST00000539145.5:c.335T>C	ENSP00000444471.1:n.335T>C
ENST00000539154.1:n.779T>C
ENST00000541159.5:c.781T>C	ENSP00000438711.1:p.Phe261Leu
ENST00000542898.5:c.1507T>C	ENSP00000444615.1:p.Phe503Leu
ENST00000570511.5:c.968T>C	ENSP00000458312.1:n.968T>C
ENST00000572244.5:c.278-642T>C	ENSP00000461186.1:n.278-642T>C
ENST00000574583.5:c.335T>C	ENSP00000460269.1:n.335T>C
ENST00000576315.5:c.335T>C	ENSP00000460551.1:n.335T>C
ENST00000621655.1:c.781T>C	ENSP00000481436.1:p.Phe261Leu
NM_000243.2:c.1414T>C , LRG_190t1:c.1414T>C	NP_000234.1:p.Phe472Leu
NM_001198536.1:c.781T>C	NP_001185465.1:p.Phe261Leu
XM_017023236.2:c.1411T>C	XP_016878725.1:p.Phe471Leu
XR_001751903.1:n.1603T>C
NM_000243.3:c.1414T>C MANE Select	NP_000234.1:p.Phe472Leu
NM_001198536.2:c.781T>C	NP_001185465.2:p.Phe261Leu