Canonical Allele Identifier: CA620713275
Gene: MEFV HGNC NCBI

Linked Data

dbSNP Id: rs1167328352

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3249668del , CM000678.2:g.3249668del GRCh38
NC_000016.9:g.3299668del , CM000678.1:g.3299668del GRCh37
NC_000016.8:g.3239669del NCBI36
NG_007871.1:g.11964del , LRG_190:g.11964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.1027del MANE Select ENSP00000219596.1:p.Gln343ArgfsTer25
ENST00000219596.5:c.1027del ENSP00000219596.1:p.Gln343ArgfsTer25
ENST00000339854.8:c.487del ENSP00000339639.4:p.Gln163ArgfsTer25
ENST00000536379.5:c.394del ENSP00000445079.1:p.Gln132ArgfsTer25
ENST00000536980.5:c.394del ENSP00000444178.1:p.Gln132ArgfsTer25
ENST00000537682.5:c.1027del ENSP00000438611.1:p.Gln343ArgfsTer25
ENST00000538326.5:c.1027del ENSP00000437486.1:p.Gln343ArgfsTer25
ENST00000539145.5:c.278-2418del ENSP00000444471.1:n.278-2418del
ENST00000541159.5:c.394del ENSP00000438711.1:p.Gln132ArgfsTer25
ENST00000542898.5:c.1120del ENSP00000444615.1:p.Gln374ArgfsTer25
ENST00000570511.5:c.911-2418del ENSP00000458312.1:n.911-2418del
ENST00000572244.5:c.278-3117del ENSP00000461186.1:n.278-3117del
ENST00000574583.5:c.278-2418del ENSP00000460269.1:n.278-2418del
ENST00000576315.5:c.278-2418del ENSP00000460551.1:n.278-2418del
ENST00000621655.1:c.394del ENSP00000481436.1:p.Gln132ArgfsTer25
NM_000243.2:c.1027del , LRG_190t1:c.1027del NP_000234.1:p.Gln343ArgfsTer25
NM_001198536.1:c.394del NP_001185465.1:p.Gln132ArgfsTer25
XM_017023236.2:c.1027del XP_016878725.1:p.Gln343ArgfsTer25
XR_001751903.1:n.1216del
NM_000243.3:c.1027del MANE Select NP_000234.1:p.Gln343ArgfsTer25
NM_001198536.2:c.394del NP_001185465.2:p.Gln132ArgfsTer25