Canonical Allele Identifier: CA280681
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97554
dbSNP Id: rs104895155
gnomAD v2: 16-3299765-G-A
gnomAD v3: 16-3249765-G-A
gnomAD v4: 16-3249765-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3249765G>A , CM000678.2:g.3249765G>A GRCh38
NC_000016.9:g.3299765G>A , CM000678.1:g.3299765G>A GRCh37
NC_000016.8:g.3239766G>A NCBI36
NG_007871.1:g.11863C>T , LRG_190:g.11863C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.926C>T MANE Select ENSP00000219596.1:p.Thr309Met
ENST00000219596.5:c.926C>T ENSP00000219596.1:p.Thr309Met
ENST00000339854.8:c.386C>T ENSP00000339639.4:p.Thr129Met
ENST00000536379.5:c.293C>T ENSP00000445079.1:p.Thr98Met
ENST00000536980.5:c.293C>T ENSP00000444178.1:p.Thr98Met
ENST00000537682.5:c.926C>T ENSP00000438611.1:p.Thr309Met
ENST00000538326.5:c.926C>T ENSP00000437486.1:p.Thr309Met
ENST00000539145.5:c.278-2519C>T ENSP00000444471.1:n.278-2519C>T
ENST00000541159.5:c.293C>T ENSP00000438711.1:p.Thr98Met
ENST00000542898.5:c.1019C>T ENSP00000444615.1:p.Thr340Met
ENST00000570511.5:c.911-2519C>T ENSP00000458312.1:n.911-2519C>T
ENST00000572244.5:c.278-3218C>T ENSP00000461186.1:n.278-3218C>T
ENST00000574583.5:c.278-2519C>T ENSP00000460269.1:n.278-2519C>T
ENST00000576315.5:c.278-2519C>T ENSP00000460551.1:n.278-2519C>T
ENST00000621655.1:c.293C>T ENSP00000481436.1:p.Thr98Met
NM_000243.2:c.926C>T , LRG_190t1:c.926C>T NP_000234.1:p.Thr309Met
NM_001198536.1:c.293C>T NP_001185465.1:p.Thr98Met
XM_017023236.2:c.926C>T XP_016878725.1:p.Thr309Met
XR_001751903.1:n.1115C>T
NM_000243.3:c.926C>T MANE Select NP_000234.1:p.Thr309Met
NM_001198536.2:c.293C>T NP_001185465.2:p.Thr98Met