Canonical Allele Identifier: CA394486860

Gene: MEFV

Linked Data

• gnomAD v4: 16-3243475-T-C
• MyVariant Identifiers: chr16:g.3293475T>C (hg19) ; chr16:g.3243475T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243475T>C , CM000678.2:g.3243475T>C	GRCh38
NC_000016.9:g.3293475T>C , CM000678.1:g.3293475T>C	GRCh37
NC_000016.8:g.3233476T>C	NCBI36
NG_007871.1:g.18153A>G , LRG_190:g.18153A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1133A>G
ENST00000219596.6:c.2012A>G MANE Select	ENSP00000219596.1:p.Lys671Arg
ENST00000219596.5:c.2012A>G	ENSP00000219596.1:p.Lys671Arg
ENST00000339854.8:c.1472A>G	ENSP00000339639.4:p.Lys491Arg
ENST00000536379.5:c.1379A>G	ENSP00000445079.1:p.Lys460Arg
ENST00000536980.5:c.*288A>G	ENSP00000444178.1:n.*288A>G
ENST00000537682.5:c.*288A>G	ENSP00000438611.1:n.*288A>G
ENST00000538326.5:c.*637A>G	ENSP00000437486.1:n.*637A>G
ENST00000539145.5:c.933A>G	ENSP00000444471.1:n.933A>G
ENST00000541159.5:c.1554A>G	ENSP00000438711.1:n.1554A>G
ENST00000542898.5:c.*288A>G	ENSP00000444615.1:n.*288A>G
ENST00000570511.5:c.1417A>G	ENSP00000458312.1:n.1417A>G
ENST00000572244.5:c.702A>G	ENSP00000461186.1:n.702A>G
ENST00000574583.5:c.784A>G	ENSP00000460269.1:n.784A>G
ENST00000576315.5:c.817A>G	ENSP00000460551.1:n.817A>G
ENST00000621655.1:c.1549A>G	ENSP00000481436.1:n.1549A>G
NM_000243.2:c.2012A>G , LRG_190t1:c.2012A>G	NP_000234.1:p.Lys671Arg
NM_001198536.1:c.*216A>G	NP_001185465.1:n.*216A>G
XM_017023236.2:c.2009A>G	XP_016878725.1:p.Lys670Arg
NM_000243.3:c.2012A>G MANE Select	NP_000234.1:p.Lys671Arg
NM_001198536.2:c.*216A>G	NP_001185465.2:n.*216A>G