Canonical Allele Identifier: CA493384000

Gene: MEFV

Linked Data

• gnomAD v4: 16-3249590-T-A
• MyVariant Identifiers: chr16:g.3299590T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3249590T>A , CM000678.2:g.3249590T>A	GRCh38
NC_000016.9:g.3299590T>A , CM000678.1:g.3299590T>A	GRCh37
NC_000016.8:g.3239591T>A	NCBI36
NG_007871.1:g.12038A>T , LRG_190:g.12038A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.1101A>T MANE Select	ENSP00000219596.1:p.Leu367=
ENST00000219596.5:c.1101A>T	ENSP00000219596.1:p.Leu367=
ENST00000339854.8:c.561A>T	ENSP00000339639.4:p.Leu187=
ENST00000536379.5:c.468A>T	ENSP00000445079.1:p.Leu156=
ENST00000536980.5:c.468A>T	ENSP00000444178.1:p.Leu156=
ENST00000537682.5:c.1101A>T	ENSP00000438611.1:p.Leu367=
ENST00000538326.5:c.1101A>T	ENSP00000437486.1:p.Leu367=
ENST00000539145.5:c.278-2344A>T	ENSP00000444471.1:n.278-2344A>T
ENST00000541159.5:c.468A>T	ENSP00000438711.1:p.Leu156=
ENST00000542898.5:c.1194A>T	ENSP00000444615.1:p.Leu398=
ENST00000570511.5:c.911-2344A>T	ENSP00000458312.1:n.911-2344A>T
ENST00000572244.5:c.278-3043A>T	ENSP00000461186.1:n.278-3043A>T
ENST00000574583.5:c.278-2344A>T	ENSP00000460269.1:n.278-2344A>T
ENST00000576315.5:c.278-2344A>T	ENSP00000460551.1:n.278-2344A>T
ENST00000621655.1:c.468A>T	ENSP00000481436.1:p.Leu156=
NM_000243.2:c.1101A>T , LRG_190t1:c.1101A>T	NP_000234.1:p.Leu367=
NM_001198536.1:c.468A>T	NP_001185465.1:p.Leu156=
XM_017023236.2:c.1101A>T	XP_016878725.1:p.Leu367=
XR_001751903.1:n.1290A>T
NM_000243.3:c.1101A>T MANE Select	NP_000234.1:p.Leu367=
NM_001198536.2:c.468A>T	NP_001185465.2:p.Leu156=