Canonical Allele Identifier: CA394471442

Gene: MEFV

Linked Data

• gnomAD v4: 16-3249705-C-A
• MyVariant Identifiers: chr16:g.3299705C>A (hg19) ; chr16:g.3249705C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3249705C>A , CM000678.2:g.3249705C>A	GRCh38
NC_000016.9:g.3299705C>A , CM000678.1:g.3299705C>A	GRCh37
NC_000016.8:g.3239706C>A	NCBI36
NG_007871.1:g.11923G>T , LRG_190:g.11923G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.986G>T MANE Select	ENSP00000219596.1:p.Arg329Leu
ENST00000219596.5:c.986G>T	ENSP00000219596.1:p.Arg329Leu
ENST00000339854.8:c.446G>T	ENSP00000339639.4:p.Arg149Leu
ENST00000536379.5:c.353G>T	ENSP00000445079.1:p.Arg118Leu
ENST00000536980.5:c.353G>T	ENSP00000444178.1:p.Arg118Leu
ENST00000537682.5:c.986G>T	ENSP00000438611.1:p.Arg329Leu
ENST00000538326.5:c.986G>T	ENSP00000437486.1:p.Arg329Leu
ENST00000539145.5:c.278-2459G>T	ENSP00000444471.1:n.278-2459G>T
ENST00000541159.5:c.353G>T	ENSP00000438711.1:p.Arg118Leu
ENST00000542898.5:c.1079G>T	ENSP00000444615.1:p.Arg360Leu
ENST00000570511.5:c.911-2459G>T	ENSP00000458312.1:n.911-2459G>T
ENST00000572244.5:c.278-3158G>T	ENSP00000461186.1:n.278-3158G>T
ENST00000574583.5:c.278-2459G>T	ENSP00000460269.1:n.278-2459G>T
ENST00000576315.5:c.278-2459G>T	ENSP00000460551.1:n.278-2459G>T
ENST00000621655.1:c.353G>T	ENSP00000481436.1:p.Arg118Leu
NM_000243.2:c.986G>T , LRG_190t1:c.986G>T	NP_000234.1:p.Arg329Leu
NM_001198536.1:c.353G>T	NP_001185465.1:p.Arg118Leu
XM_017023236.2:c.986G>T	XP_016878725.1:p.Arg329Leu
XR_001751903.1:n.1175G>T
NM_000243.3:c.986G>T MANE Select	NP_000234.1:p.Arg329Leu
NM_001198536.2:c.353G>T	NP_001185465.2:p.Arg118Leu