Canonical Allele Identifier: CA973876853
Gene: MEFV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3254483_3254515dup , CM000678.2:g.3254483_3254515dup GRCh38
NC_000016.9:g.3304483_3304515dup , CM000678.1:g.3304483_3304515dup GRCh37
NC_000016.8:g.3244484_3244516dup NCBI36
NG_007871.1:g.7116_7148dup , LRG_190:g.7116_7148dup

Transcript Alleles

HGVS Amino-acid change
ENST00000219596.6:c.556_588dup MANE Select ENSP00000219596.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaL...
ENST00000219596.5:c.556_588dup ENSP00000219596.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaL...
ENST00000339854.8:c.277+1799_277+1831dup ENSP00000339639.4:n.277+1799_277+1831dup
ENST00000536379.5:c.277+1799_277+1831dup ENSP00000445079.1:n.277+1799_277+1831dup
ENST00000536980.5:c.277+1799_277+1831dup ENSP00000444178.1:n.277+1799_277+1831dup
ENST00000537682.5:c.556_588dup ENSP00000438611.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaL...
ENST00000538326.5:c.556_588dup ENSP00000437486.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaL...
ENST00000539145.5:c.277+1799_277+1831dup ENSP00000444471.1:n.277+1799_277+1831dup
ENST00000541159.5:c.277+1799_277+1831dup ENSP00000438711.1:n.277+1799_277+1831dup
ENST00000542898.5:c.556_588dup ENSP00000444615.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaL...
ENST00000570511.5:c.556_588dup ENSP00000458312.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaL...
ENST00000572244.5:c.277+1799_277+1831dup ENSP00000461186.1:n.277+1799_277+1831dup
ENST00000574583.5:c.277+1799_277+1831dup ENSP00000460269.1:n.277+1799_277+1831dup
ENST00000576315.5:c.277+1799_277+1831dup ENSP00000460551.1:n.277+1799_277+1831dup
ENST00000621655.1:c.277+1799_277+1831dup ENSP00000481436.1:n.277+1799_277+1831dup
NM_000243.2:c.556_588dup , LRG_190t1:c.556_588dup NP_000234.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaLeuGluG...
NM_001198536.1:c.277+1799_277+1831dup NP_001185465.1:n.277+1799_277+1831dup
XM_017023236.2:c.556_588dup XP_016878725.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaLeuG...
XR_001751903.1:n.745_777dup
NM_000243.3:c.556_588dup MANE Select NP_000234.1:p.Gly196_Gly197insArgSerProGlyProCysArgAlaLeuGluG...
NM_001198536.2:c.277+1799_277+1831dup NP_001185465.2:n.277+1799_277+1831dup