Canonical Allele Identifier: CA2202659249
Gene: MEFV HGNC NCBI

Linked Data

dbSNP Id: rs1958910737

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3244546_3244547del , CM000678.2:g.3244546_3244547del GRCh38
NC_000016.9:g.3294546_3294547del , CM000678.1:g.3294546_3294547del GRCh37
NC_000016.8:g.3234547_3234548del NCBI36
NG_007871.1:g.17081_17082del , LRG_190:g.17081_17082del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.773_774del
ENST00000219596.6:c.1652_1653del MANE Select ENSP00000219596.1:p.Gln551ArgfsTer?
ENST00000219596.5:c.1652_1653del ENSP00000219596.1:p.Gln551ArgfsTer?
ENST00000339854.8:c.1112_1113del ENSP00000339639.4:p.Gln371ArgfsTer?
ENST00000536379.5:c.1019_1020del ENSP00000445079.1:p.Gln340ArgfsTer?
ENST00000536980.5:c.1019_1020del ENSP00000444178.1:p.Gln340ArgfsTer?
ENST00000537682.5:c.1652_1653del ENSP00000438611.1:p.Gln551ArgfsTer?
ENST00000538326.5:c.*277_*278del ENSP00000437486.1:n.*277_*278del
ENST00000539145.5:c.573_574del ENSP00000444471.1:n.573_574del
ENST00000541159.5:c.1019_1020del ENSP00000438711.1:p.Gln340ArgfsTer?
ENST00000542898.5:c.1745_1746del ENSP00000444615.1:p.Gln582ArgfsTer?
ENST00000570511.5:c.1165-655_1165-654del ENSP00000458312.1:n.1165-655_1165-654del
ENST00000572244.5:c.342_343del ENSP00000461186.1:n.342_343del
ENST00000574583.5:c.532-655_532-654del ENSP00000460269.1:n.532-655_532-654del
ENST00000576315.5:c.532-261_532-260del ENSP00000460551.1:n.532-261_532-260del
ENST00000621655.1:c.1019_1020del ENSP00000481436.1:p.Gln340ArgfsTer?
NM_000243.2:c.1652_1653del , LRG_190t1:c.1652_1653del NP_000234.1:p.Gln551ArgfsTer?
NM_001198536.1:c.1019_1020del NP_001185465.1:p.Gln340ArgfsTer?
XM_017023236.2:c.1649_1650del XP_016878725.1:p.Gln550ArgfsTer?
XR_001751903.1:n.1841_1842del
NM_000243.3:c.1652_1653del MANE Select NP_000234.1:p.Gln551ArgfsTer?
NM_001198536.2:c.1019_1020del NP_001185465.2:p.Gln340ArgfsTer?