Canonical Allele Identifier: CA394490489

Gene: MEFV

Linked Data

• gnomAD v4: 16-3244278-G-T
• MyVariant Identifiers: chr16:g.3294278G>T (hg19) ; chr16:g.3244278G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244278G>T , CM000678.2:g.3244278G>T	GRCh38
NC_000016.9:g.3294278G>T , CM000678.1:g.3294278G>T	GRCh37
NC_000016.8:g.3234279G>T	NCBI36
NG_007871.1:g.17350C>A , LRG_190:g.17350C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.856C>A
ENST00000219596.6:c.1735C>A MANE Select	ENSP00000219596.1:p.Arg579Ser
ENST00000219596.5:c.1735C>A	ENSP00000219596.1:p.Arg579Ser
ENST00000339854.8:c.1195C>A	ENSP00000339639.4:p.Arg399Ser
ENST00000536379.5:c.1102C>A	ENSP00000445079.1:p.Arg368Ser
ENST00000536980.5:c.1102C>A	ENSP00000444178.1:p.Arg368Ser
ENST00000537682.5:c.1735C>A	ENSP00000438611.1:p.Arg579Ser
ENST00000538326.5:c.*360C>A	ENSP00000437486.1:n.*360C>A
ENST00000539145.5:c.656C>A	ENSP00000444471.1:n.656C>A
ENST00000541159.5:c.1102C>A	ENSP00000438711.1:p.Arg368Ser
ENST00000542898.5:c.1828C>A	ENSP00000444615.1:p.Arg610Ser
ENST00000570511.5:c.1165-386C>A	ENSP00000458312.1:n.1165-386C>A
ENST00000572244.5:c.425C>A	ENSP00000461186.1:n.425C>A
ENST00000574583.5:c.532-386C>A	ENSP00000460269.1:n.532-386C>A
ENST00000576315.5:c.540C>A	ENSP00000460551.1:n.540C>A
ENST00000621655.1:c.1102C>A	ENSP00000481436.1:p.Arg368Ser
NM_000243.2:c.1735C>A , LRG_190t1:c.1735C>A	NP_000234.1:p.Arg579Ser
NM_001198536.1:c.1102C>A	NP_001185465.1:p.Arg368Ser
XM_017023236.2:c.1732C>A	XP_016878725.1:p.Arg578Ser
XR_001751903.1:n.1924C>A
NM_000243.3:c.1735C>A MANE Select	NP_000234.1:p.Arg579Ser
NM_001198536.2:c.1102C>A	NP_001185465.2:p.Arg368Ser