Canonical Allele Identifier: CA2202658577
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243280G= , CM000678.2:g.3243280G= GRCh38
NC_000016.9:g.3293280G= , CM000678.1:g.3293280G= GRCh37
NC_000016.8:g.3233281G= NCBI36
NG_007871.1:g.18348C= , LRG_190:g.18348C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1328C=
ENST00000219596.6:c.2207C= MANE Select ENSP00000219596.1:p.Ala736=
ENST00000219596.5:c.2207C= ENSP00000219596.1:p.Ala736=
ENST00000339854.8:c.1667C= ENSP00000339639.4:p.Ala556=
ENST00000536379.5:c.1574C= ENSP00000445079.1:p.Ala525=
ENST00000536980.5:c.*483C= ENSP00000444178.1:n.*483C=
ENST00000537682.5:c.*483C= ENSP00000438611.1:n.*483C=
ENST00000538326.5:c.*832C= ENSP00000437486.1:n.*832C=
ENST00000539145.5:c.1128C= ENSP00000444471.1:n.1128C=
ENST00000541159.5:c.1749C= ENSP00000438711.1:n.1749C=
ENST00000542898.5:c.*483C= ENSP00000444615.1:n.*483C=
ENST00000570511.5:c.1612C= ENSP00000458312.1:n.1612C=
ENST00000572244.5:c.897C= ENSP00000461186.1:n.897C=
ENST00000574583.5:c.979C= ENSP00000460269.1:n.979C=
ENST00000576315.5:c.1012C= ENSP00000460551.1:n.1012C=
ENST00000621655.1:c.1744C= ENSP00000481436.1:n.1744C=
NM_000243.2:c.2207C= , LRG_190t1:c.2207C= NP_000234.1:p.Ala736=
NM_001198536.1:c.*411C= NP_001185465.1:n.*411C=
XM_017023236.2:c.2204C= XP_016878725.1:p.Ala735=
NM_000243.3:c.2207C= MANE Select NP_000234.1:p.Ala736=
NM_001198536.2:c.*411C= NP_001185465.2:n.*411C=