Canonical Allele Identifier: CA2202658714
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243549C= , CM000678.2:g.3243549C= GRCh38
NC_000016.9:g.3293549C= , CM000678.1:g.3293549C= GRCh37
NC_000016.8:g.3233550C= NCBI36
NG_007871.1:g.18079G= , LRG_190:g.18079G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1059G=
ENST00000219596.6:c.1938G= MANE Select ENSP00000219596.1:p.Pro646=
ENST00000219596.5:c.1938G= ENSP00000219596.1:p.Pro646=
ENST00000339854.8:c.1398G= ENSP00000339639.4:p.Pro466=
ENST00000536379.5:c.1305G= ENSP00000445079.1:p.Pro435=
ENST00000536980.5:c.*214G= ENSP00000444178.1:n.*214G=
ENST00000537682.5:c.*214G= ENSP00000438611.1:n.*214G=
ENST00000538326.5:c.*563G= ENSP00000437486.1:n.*563G=
ENST00000539145.5:c.859G= ENSP00000444471.1:n.859G=
ENST00000541159.5:c.1480G= ENSP00000438711.1:n.1480G=
ENST00000542898.5:c.*214G= ENSP00000444615.1:n.*214G=
ENST00000570511.5:c.1343G= ENSP00000458312.1:n.1343G=
ENST00000572244.5:c.628G= ENSP00000461186.1:n.628G=
ENST00000574583.5:c.710G= ENSP00000460269.1:n.710G=
ENST00000576315.5:c.743G= ENSP00000460551.1:n.743G=
ENST00000621655.1:c.1475G= ENSP00000481436.1:n.1475G=
NM_000243.2:c.1938G= , LRG_190t1:c.1938G= NP_000234.1:p.Pro646=
NM_001198536.1:c.*142G= NP_001185465.1:n.*142G=
XM_017023236.2:c.1935G= XP_016878725.1:p.Pro645=
NM_000243.3:c.1938G= MANE Select NP_000234.1:p.Pro646=
NM_001198536.2:c.*142G= NP_001185465.2:n.*142G=