Canonical Allele Identifier: CA2202658676
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243455C= , CM000678.2:g.3243455C= GRCh38
NC_000016.9:g.3293455C= , CM000678.1:g.3293455C= GRCh37
NC_000016.8:g.3233456C= NCBI36
NG_007871.1:g.18173G= , LRG_190:g.18173G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1153G=
ENST00000219596.6:c.2032G= MANE Select ENSP00000219596.1:p.Gly678=
ENST00000219596.5:c.2032G= ENSP00000219596.1:p.Gly678=
ENST00000339854.8:c.1492G= ENSP00000339639.4:p.Gly498=
ENST00000536379.5:c.1399G= ENSP00000445079.1:p.Gly467=
ENST00000536980.5:c.*308G= ENSP00000444178.1:n.*308G=
ENST00000537682.5:c.*308G= ENSP00000438611.1:n.*308G=
ENST00000538326.5:c.*657G= ENSP00000437486.1:n.*657G=
ENST00000539145.5:c.953G= ENSP00000444471.1:n.953G=
ENST00000541159.5:c.1574G= ENSP00000438711.1:n.1574G=
ENST00000542898.5:c.*308G= ENSP00000444615.1:n.*308G=
ENST00000570511.5:c.1437G= ENSP00000458312.1:n.1437G=
ENST00000572244.5:c.722G= ENSP00000461186.1:n.722G=
ENST00000574583.5:c.804G= ENSP00000460269.1:n.804G=
ENST00000576315.5:c.837G= ENSP00000460551.1:n.837G=
ENST00000621655.1:c.1569G= ENSP00000481436.1:n.1569G=
NM_000243.2:c.2032G= , LRG_190t1:c.2032G= NP_000234.1:p.Gly678=
NM_001198536.1:c.*236G= NP_001185465.1:n.*236G=
XM_017023236.2:c.2029G= XP_016878725.1:p.Gly677=
NM_000243.3:c.2032G= MANE Select NP_000234.1:p.Gly678=
NM_001198536.2:c.*236G= NP_001185465.2:n.*236G=