Canonical Allele Identifier: CA2202658599
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243329T= , CM000678.2:g.3243329T= GRCh38
NC_000016.9:g.3293329T= , CM000678.1:g.3293329T= GRCh37
NC_000016.8:g.3233330T= NCBI36
NG_007871.1:g.18299A= , LRG_190:g.18299A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1279A=
ENST00000219596.6:c.2158A= MANE Select ENSP00000219596.1:p.Ile720=
ENST00000219596.5:c.2158A= ENSP00000219596.1:p.Ile720=
ENST00000339854.8:c.1618A= ENSP00000339639.4:p.Ile540=
ENST00000536379.5:c.1525A= ENSP00000445079.1:p.Ile509=
ENST00000536980.5:c.*434A= ENSP00000444178.1:n.*434A=
ENST00000537682.5:c.*434A= ENSP00000438611.1:n.*434A=
ENST00000538326.5:c.*783A= ENSP00000437486.1:n.*783A=
ENST00000539145.5:c.1079A= ENSP00000444471.1:n.1079A=
ENST00000541159.5:c.1700A= ENSP00000438711.1:n.1700A=
ENST00000542898.5:c.*434A= ENSP00000444615.1:n.*434A=
ENST00000570511.5:c.1563A= ENSP00000458312.1:n.1563A=
ENST00000572244.5:c.848A= ENSP00000461186.1:n.848A=
ENST00000574583.5:c.930A= ENSP00000460269.1:n.930A=
ENST00000576315.5:c.963A= ENSP00000460551.1:n.963A=
ENST00000621655.1:c.1695A= ENSP00000481436.1:n.1695A=
NM_000243.2:c.2158A= , LRG_190t1:c.2158A= NP_000234.1:p.Ile720=
NM_001198536.1:c.*362A= NP_001185465.1:n.*362A=
XM_017023236.2:c.2155A= XP_016878725.1:p.Ile719=
NM_000243.3:c.2158A= MANE Select NP_000234.1:p.Ile720=
NM_001198536.2:c.*362A= NP_001185465.2:n.*362A=