Canonical Allele Identifier: CA394459164
Gene: MEFV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3244584T>A , CM000678.2:g.3244584T>A GRCh38
NC_000016.9:g.3294584T>A , CM000678.1:g.3294584T>A GRCh37
NC_000016.8:g.3234585T>A NCBI36
NG_007871.1:g.17044A>T , LRG_190:g.17044A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.736A>T
ENST00000219596.6:c.1615A>T MANE Select ENSP00000219596.1:p.Lys539Ter
ENST00000219596.5:c.1615A>T ENSP00000219596.1:p.Lys539Ter
ENST00000339854.8:c.1075A>T ENSP00000339639.4:p.Lys359Ter
ENST00000536379.5:c.982A>T ENSP00000445079.1:p.Lys328Ter
ENST00000536980.5:c.982A>T ENSP00000444178.1:p.Lys328Ter
ENST00000537682.5:c.1615A>T ENSP00000438611.1:p.Lys539Ter
ENST00000538326.5:c.*240A>T ENSP00000437486.1:n.*240A>T
ENST00000539145.5:c.536A>T ENSP00000444471.1:n.536A>T
ENST00000541159.5:c.982A>T ENSP00000438711.1:p.Lys328Ter
ENST00000542898.5:c.1708A>T ENSP00000444615.1:p.Lys570Ter
ENST00000570511.5:c.1165-692A>T ENSP00000458312.1:n.1165-692A>T
ENST00000572244.5:c.305A>T ENSP00000461186.1:p.Ter102Leu
ENST00000574583.5:c.532-692A>T ENSP00000460269.1:n.532-692A>T
ENST00000576315.5:c.532-298A>T ENSP00000460551.1:n.532-298A>T
ENST00000621655.1:c.982A>T ENSP00000481436.1:p.Lys328Ter
NM_000243.2:c.1615A>T , LRG_190t1:c.1615A>T NP_000234.1:p.Lys539Ter
NM_001198536.1:c.982A>T NP_001185465.1:p.Lys328Ter
XM_017023236.2:c.1612A>T XP_016878725.1:p.Lys538Ter
XR_001751903.1:n.1804A>T
NM_000243.3:c.1615A>T MANE Select NP_000234.1:p.Lys539Ter
NM_001198536.2:c.982A>T NP_001185465.2:p.Lys328Ter