Canonical Allele Identifier: CA2631353161
Gene: MEFV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3249889_3249890del , CM000678.2:g.3249889_3249890del GRCh38
NC_000016.9:g.3299889_3299890del , CM000678.1:g.3299889_3299890del GRCh37
NC_000016.8:g.3239890_3239891del NCBI36
NG_007871.1:g.11738_11739del , LRG_190:g.11738_11739del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.911-110_911-109del MANE Select ENSP00000219596.1:n.911-110_911-109del
ENST00000219596.5:c.911-110_911-109del ENSP00000219596.1:n.911-110_911-109del
ENST00000339854.8:c.371-110_371-109del ENSP00000339639.4:n.371-110_371-109del
ENST00000536379.5:c.278-110_278-109del ENSP00000445079.1:n.278-110_278-109del
ENST00000536980.5:c.278-110_278-109del ENSP00000444178.1:n.278-110_278-109del
ENST00000537682.5:c.911-110_911-109del ENSP00000438611.1:n.911-110_911-109del
ENST00000538326.5:c.911-110_911-109del ENSP00000437486.1:n.911-110_911-109del
ENST00000539145.5:c.278-2644_278-2643del ENSP00000444471.1:n.278-2644_278-2643del
ENST00000541159.5:c.278-110_278-109del ENSP00000438711.1:n.278-110_278-109del
ENST00000542898.5:c.1004-110_1004-109del ENSP00000444615.1:n.1004-110_1004-109del
ENST00000570511.5:c.911-2644_911-2643del ENSP00000458312.1:n.911-2644_911-2643del
ENST00000572244.5:c.278-3343_278-3342del ENSP00000461186.1:n.278-3343_278-3342del
ENST00000574583.5:c.278-2644_278-2643del ENSP00000460269.1:n.278-2644_278-2643del
ENST00000576315.5:c.278-2644_278-2643del ENSP00000460551.1:n.278-2644_278-2643del
ENST00000621655.1:c.278-110_278-109del ENSP00000481436.1:n.278-110_278-109del
NM_000243.2:c.911-110_911-109del , LRG_190t1:c.911-110_911-109del NP_000234.1:n.911-110_911-109del
NM_001198536.1:c.278-110_278-109del NP_001185465.1:n.278-110_278-109del
XM_017023236.2:c.911-110_911-109del XP_016878725.1:n.911-110_911-109del
XR_001751903.1:n.1100-110_1100-109del
NM_000243.3:c.911-110_911-109del MANE Select NP_000234.1:n.911-110_911-109del
NM_001198536.2:c.278-110_278-109del NP_001185465.2:n.278-110_278-109del