Canonical Allele Identifier: CA2202658626
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243370G= , CM000678.2:g.3243370G= GRCh38
NC_000016.9:g.3293370G= , CM000678.1:g.3293370G= GRCh37
NC_000016.8:g.3233371G= NCBI36
NG_007871.1:g.18258C= , LRG_190:g.18258C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1238C=
ENST00000219596.6:c.2117C= MANE Select ENSP00000219596.1:p.Pro706=
ENST00000219596.5:c.2117C= ENSP00000219596.1:p.Pro706=
ENST00000339854.8:c.1577C= ENSP00000339639.4:p.Pro526=
ENST00000536379.5:c.1484C= ENSP00000445079.1:p.Pro495=
ENST00000536980.5:c.*393C= ENSP00000444178.1:n.*393C=
ENST00000537682.5:c.*393C= ENSP00000438611.1:n.*393C=
ENST00000538326.5:c.*742C= ENSP00000437486.1:n.*742C=
ENST00000539145.5:c.1038C= ENSP00000444471.1:n.1038C=
ENST00000541159.5:c.1659C= ENSP00000438711.1:n.1659C=
ENST00000542898.5:c.*393C= ENSP00000444615.1:n.*393C=
ENST00000570511.5:c.1522C= ENSP00000458312.1:n.1522C=
ENST00000572244.5:c.807C= ENSP00000461186.1:n.807C=
ENST00000574583.5:c.889C= ENSP00000460269.1:n.889C=
ENST00000576315.5:c.922C= ENSP00000460551.1:n.922C=
ENST00000621655.1:c.1654C= ENSP00000481436.1:n.1654C=
NM_000243.2:c.2117C= , LRG_190t1:c.2117C= NP_000234.1:p.Pro706=
NM_001198536.1:c.*321C= NP_001185465.1:n.*321C=
XM_017023236.2:c.2114C= XP_016878725.1:p.Pro705=
NM_000243.3:c.2117C= MANE Select NP_000234.1:p.Pro706=
NM_001198536.2:c.*321C= NP_001185465.2:n.*321C=