Canonical Allele Identifier: CA493383599

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293282T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243282T>G , CM000678.2:g.3243282T>G	GRCh38
NC_000016.9:g.3293282T>G , CM000678.1:g.3293282T>G	GRCh37
NC_000016.8:g.3233283T>G	NCBI36
NG_007871.1:g.18346A>C , LRG_190:g.18346A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1326A>C
ENST00000219596.6:c.2205A>C MANE Select	ENSP00000219596.1:p.Thr735=
ENST00000219596.5:c.2205A>C	ENSP00000219596.1:p.Thr735=
ENST00000339854.8:c.1665A>C	ENSP00000339639.4:p.Thr555=
ENST00000536379.5:c.1572A>C	ENSP00000445079.1:p.Thr524=
ENST00000536980.5:c.*481A>C	ENSP00000444178.1:n.*481A>C
ENST00000537682.5:c.*481A>C	ENSP00000438611.1:n.*481A>C
ENST00000538326.5:c.*830A>C	ENSP00000437486.1:n.*830A>C
ENST00000539145.5:c.1126A>C	ENSP00000444471.1:n.1126A>C
ENST00000541159.5:c.1747A>C	ENSP00000438711.1:n.1747A>C
ENST00000542898.5:c.*481A>C	ENSP00000444615.1:n.*481A>C
ENST00000570511.5:c.1610A>C	ENSP00000458312.1:n.1610A>C
ENST00000572244.5:c.895A>C	ENSP00000461186.1:n.895A>C
ENST00000574583.5:c.977A>C	ENSP00000460269.1:n.977A>C
ENST00000576315.5:c.1010A>C	ENSP00000460551.1:n.1010A>C
ENST00000621655.1:c.1742A>C	ENSP00000481436.1:n.1742A>C
NM_000243.2:c.2205A>C , LRG_190t1:c.2205A>C	NP_000234.1:p.Thr735=
NM_001198536.1:c.*409A>C	NP_001185465.1:n.*409A>C
XM_017023236.2:c.2202A>C	XP_016878725.1:p.Thr734=
NM_000243.3:c.2205A>C MANE Select	NP_000234.1:p.Thr735=
NM_001198536.2:c.*409A>C	NP_001185465.2:n.*409A>C