Canonical Allele Identifier: CA2631355299

Gene: MEFV

Linked Data

• gnomAD v4: 16-3254625-TCGGGCTGGCTGCACCGCAGGCTGGCAGCTCCGCCCCCGTACGGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3254626_3254670del , CM000678.2:g.3254626_3254670del	GRCh38
NC_000016.9:g.3304626_3304670del , CM000678.1:g.3304626_3304670del	GRCh37
NC_000016.8:g.3244627_3244671del	NCBI36
NG_007871.1:g.6958_7002del , LRG_190:g.6958_7002del

Transcript Alleles

HGVS	Amino-acid change
ENST00000219596.6:c.398_442del MANE Select	ENSP00000219596.1:p.Arg133_Glu148delinsGl...
ENST00000219596.5:c.398_442del	ENSP00000219596.1:p.Arg133_Glu148delinsGl...
ENST00000339854.8:c.277+1641_277+1685del	ENSP00000339639.4:n.277+1641_277+1685del
ENST00000536379.5:c.277+1641_277+1685del	ENSP00000445079.1:n.277+1641_277+1685del
ENST00000536980.5:c.277+1641_277+1685del	ENSP00000444178.1:n.277+1641_277+1685del
ENST00000537682.5:c.398_442del	ENSP00000438611.1:p.Arg133_Glu148delinsGl...
ENST00000538326.5:c.398_442del	ENSP00000437486.1:p.Arg133_Glu148delinsGl...
ENST00000539145.5:c.277+1641_277+1685del	ENSP00000444471.1:n.277+1641_277+1685del
ENST00000541159.5:c.277+1641_277+1685del	ENSP00000438711.1:n.277+1641_277+1685del
ENST00000542898.5:c.398_442del	ENSP00000444615.1:p.Arg133_Glu148delinsGl...
ENST00000570511.5:c.398_442del	ENSP00000458312.1:p.Arg133_Glu148delinsGl...
ENST00000572244.5:c.277+1641_277+1685del	ENSP00000461186.1:n.277+1641_277+1685del
ENST00000574583.5:c.277+1641_277+1685del	ENSP00000460269.1:n.277+1641_277+1685del
ENST00000576315.5:c.277+1641_277+1685del	ENSP00000460551.1:n.277+1641_277+1685del
ENST00000621655.1:c.277+1641_277+1685del	ENSP00000481436.1:n.277+1641_277+1685del
NM_000243.2:c.398_442del , LRG_190t1:c.398_442del	NP_000234.1:p.Arg133_Glu148delinsGln
NM_001198536.1:c.277+1641_277+1685del	NP_001185465.1:n.277+1641_277+1685del
XM_017023236.2:c.398_442del	XP_016878725.1:p.Arg133_Glu148delinsGln
XR_001751903.1:n.587_631del
NM_000243.3:c.398_442del MANE Select	NP_000234.1:p.Arg133_Glu148delinsGln
NM_001198536.2:c.277+1641_277+1685del	NP_001185465.2:n.277+1641_277+1685del