Canonical Allele Identifier: CA2202662079
Gene: MEFV HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000219596.6:c.926C= MANE Select ENSP00000219596.1:p.Thr309=
ENST00000219596.5:c.926C= ENSP00000219596.1:p.Thr309=
ENST00000339854.8:c.386C= ENSP00000339639.4:p.Thr129=
ENST00000536379.5:c.293C= ENSP00000445079.1:p.Thr98=
ENST00000536980.5:c.293C= ENSP00000444178.1:p.Thr98=
ENST00000537682.5:c.926C= ENSP00000438611.1:p.Thr309=
ENST00000538326.5:c.926C= ENSP00000437486.1:p.Thr309=
ENST00000539145.5:c.278-2519C= ENSP00000444471.1:n.278-2519C=
ENST00000541159.5:c.293C= ENSP00000438711.1:p.Thr98=
ENST00000542898.5:c.1019C= ENSP00000444615.1:p.Thr340=
ENST00000570511.5:c.911-2519C= ENSP00000458312.1:n.911-2519C=
ENST00000572244.5:c.278-3218C= ENSP00000461186.1:n.278-3218C=
ENST00000574583.5:c.278-2519C= ENSP00000460269.1:n.278-2519C=
ENST00000576315.5:c.278-2519C= ENSP00000460551.1:n.278-2519C=
ENST00000621655.1:c.293C= ENSP00000481436.1:p.Thr98=
NM_000243.2:c.926C= , LRG_190t1:c.926C= NP_000234.1:p.Thr309=
NM_001198536.1:c.293C= NP_001185465.1:p.Thr98=
XM_017023236.2:c.926C= XP_016878725.1:p.Thr309=
XR_001751903.1:n.1115C=
NM_000243.3:c.926C= MANE Select NP_000234.1:p.Thr309=
NM_001198536.2:c.293C= NP_001185465.2:p.Thr98=