Canonical Allele Identifier: CA2841256026
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3254239dup , CM000678.2:g.3254239dup GRCh38
NC_000016.9:g.3304239dup , CM000678.1:g.3304239dup GRCh37
NC_000016.8:g.3244240dup NCBI36
NG_007871.1:g.7392dup , LRG_190:g.7392dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.832dup MANE Select ENSP00000219596.1:p.Arg278ProfsTer?
ENST00000219596.5:c.832dup ENSP00000219596.1:p.Arg278ProfsTer?
ENST00000339854.8:c.277+2075dup ENSP00000339639.4:n.277+2075dup
ENST00000536379.5:c.277+2075dup ENSP00000445079.1:n.277+2075dup
ENST00000536980.5:c.277+2075dup ENSP00000444178.1:n.277+2075dup
ENST00000537682.5:c.832dup ENSP00000438611.1:p.Arg278ProfsTer?
ENST00000538326.5:c.832dup ENSP00000437486.1:p.Arg278ProfsTer?
ENST00000539145.5:c.277+2075dup ENSP00000444471.1:n.277+2075dup
ENST00000541159.5:c.277+2075dup ENSP00000438711.1:n.277+2075dup
ENST00000542898.5:c.832dup ENSP00000444615.1:p.Arg278ProfsTer?
ENST00000570511.5:c.832dup ENSP00000458312.1:p.Arg278ProfsTer?
ENST00000572244.5:c.277+2075dup ENSP00000461186.1:n.277+2075dup
ENST00000574583.5:c.277+2075dup ENSP00000460269.1:n.277+2075dup
ENST00000576315.5:c.277+2075dup ENSP00000460551.1:n.277+2075dup
ENST00000621655.1:c.277+2075dup ENSP00000481436.1:n.277+2075dup
NM_000243.2:c.832dup , LRG_190t1:c.832dup NP_000234.1:p.Arg278ProfsTer?
NM_001198536.1:c.277+2075dup NP_001185465.1:n.277+2075dup
XM_017023236.2:c.832dup XP_016878725.1:p.Arg278ProfsTer?
XR_001751903.1:n.1021dup
NM_000243.3:c.832dup MANE Select NP_000234.1:p.Arg278ProfsTer?
NM_001198536.2:c.277+2075dup NP_001185465.2:n.277+2075dup