Canonical Allele Identifier: CA2631355279

Gene: MEFV

Linked Data

• gnomAD v4: 16-3254620-C-CGGCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3254621_3254625dup , CM000678.2:g.3254621_3254625dup	GRCh38
NC_000016.9:g.3304621_3304625dup , CM000678.1:g.3304621_3304625dup	GRCh37
NC_000016.8:g.3244622_3244626dup	NCBI36
NG_007871.1:g.7003_7007dup , LRG_190:g.7003_7007dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.443_447dup MANE Select	ENSP00000219596.1:p.Gly150ArgfsTer11
ENST00000219596.5:c.443_447dup	ENSP00000219596.1:p.Gly150ArgfsTer11
ENST00000339854.8:c.277+1686_277+1690dup	ENSP00000339639.4:n.277+1686_277+1690dup
ENST00000536379.5:c.277+1686_277+1690dup	ENSP00000445079.1:n.277+1686_277+1690dup
ENST00000536980.5:c.277+1686_277+1690dup	ENSP00000444178.1:n.277+1686_277+1690dup
ENST00000537682.5:c.443_447dup	ENSP00000438611.1:p.Gly150ArgfsTer11
ENST00000538326.5:c.443_447dup	ENSP00000437486.1:p.Gly150ArgfsTer11
ENST00000539145.5:c.277+1686_277+1690dup	ENSP00000444471.1:n.277+1686_277+1690dup
ENST00000541159.5:c.277+1686_277+1690dup	ENSP00000438711.1:n.277+1686_277+1690dup
ENST00000542898.5:c.443_447dup	ENSP00000444615.1:p.Gly150ArgfsTer11
ENST00000570511.5:c.443_447dup	ENSP00000458312.1:p.Gly150ArgfsTer11
ENST00000572244.5:c.277+1686_277+1690dup	ENSP00000461186.1:n.277+1686_277+1690dup
ENST00000574583.5:c.277+1686_277+1690dup	ENSP00000460269.1:n.277+1686_277+1690dup
ENST00000576315.5:c.277+1686_277+1690dup	ENSP00000460551.1:n.277+1686_277+1690dup
ENST00000621655.1:c.277+1686_277+1690dup	ENSP00000481436.1:n.277+1686_277+1690dup
NM_000243.2:c.443_447dup , LRG_190t1:c.443_447dup	NP_000234.1:p.Gly150ArgfsTer11
NM_001198536.1:c.277+1686_277+1690dup	NP_001185465.1:n.277+1686_277+1690dup
XM_017023236.2:c.443_447dup	XP_016878725.1:p.Gly150ArgfsTer11
XR_001751903.1:n.632_636dup
NM_000243.3:c.443_447dup MANE Select	NP_000234.1:p.Gly150ArgfsTer11
NM_001198536.2:c.277+1686_277+1690dup	NP_001185465.2:n.277+1686_277+1690dup