Canonical Allele Identifier: CA394486710

Gene: MEFV

Linked Data

• dbSNP Id: rs1340996058
• gnomAD v2: 16-3293461-T-C
• gnomAD v4: 16-3243461-T-C
• MyVariant Identifiers: chr16:g.3293461T>C (hg19) ; chr16:g.3243461T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243461T>C , CM000678.2:g.3243461T>C	GRCh38
NC_000016.9:g.3293461T>C , CM000678.1:g.3293461T>C	GRCh37
NC_000016.8:g.3233462T>C	NCBI36
NG_007871.1:g.18167A>G , LRG_190:g.18167A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1147A>G
ENST00000219596.6:c.2026A>G MANE Select	ENSP00000219596.1:p.Arg676Gly
ENST00000219596.5:c.2026A>G	ENSP00000219596.1:p.Arg676Gly
ENST00000339854.8:c.1486A>G	ENSP00000339639.4:p.Arg496Gly
ENST00000536379.5:c.1393A>G	ENSP00000445079.1:p.Arg465Gly
ENST00000536980.5:c.*302A>G	ENSP00000444178.1:n.*302A>G
ENST00000537682.5:c.*302A>G	ENSP00000438611.1:n.*302A>G
ENST00000538326.5:c.*651A>G	ENSP00000437486.1:n.*651A>G
ENST00000539145.5:c.947A>G	ENSP00000444471.1:n.947A>G
ENST00000541159.5:c.1568A>G	ENSP00000438711.1:n.1568A>G
ENST00000542898.5:c.*302A>G	ENSP00000444615.1:n.*302A>G
ENST00000570511.5:c.1431A>G	ENSP00000458312.1:n.1431A>G
ENST00000572244.5:c.716A>G	ENSP00000461186.1:n.716A>G
ENST00000574583.5:c.798A>G	ENSP00000460269.1:n.798A>G
ENST00000576315.5:c.831A>G	ENSP00000460551.1:n.831A>G
ENST00000621655.1:c.1563A>G	ENSP00000481436.1:n.1563A>G
NM_000243.2:c.2026A>G , LRG_190t1:c.2026A>G	NP_000234.1:p.Arg676Gly
NM_001198536.1:c.*230A>G	NP_001185465.1:n.*230A>G
XM_017023236.2:c.2023A>G	XP_016878725.1:p.Arg675Gly
NM_000243.3:c.2026A>G MANE Select	NP_000234.1:p.Arg676Gly
NM_001198536.2:c.*230A>G	NP_001185465.2:n.*230A>G