Canonical Allele Identifier: CA2202658544
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243222G= , CM000678.2:g.3243222G= GRCh38
NC_000016.9:g.3293222G= , CM000678.1:g.3293222G= GRCh37
NC_000016.8:g.3233223G= NCBI36
NG_007871.1:g.18406C= , LRG_190:g.18406C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1386C=
ENST00000219596.6:c.2265C= MANE Select ENSP00000219596.1:p.Ile755=
ENST00000219596.5:c.2265C= ENSP00000219596.1:p.Ile755=
ENST00000339854.8:c.1725C= ENSP00000339639.4:p.Ile575=
ENST00000536379.5:c.1632C= ENSP00000445079.1:p.Ile544=
ENST00000536980.5:c.*541C= ENSP00000444178.1:n.*541C=
ENST00000537682.5:c.*541C= ENSP00000438611.1:n.*541C=
ENST00000538326.5:c.*890C= ENSP00000437486.1:n.*890C=
ENST00000539145.5:c.1186C= ENSP00000444471.1:n.1186C=
ENST00000541159.5:c.1807C= ENSP00000438711.1:n.1807C=
ENST00000542898.5:c.*541C= ENSP00000444615.1:n.*541C=
ENST00000570511.5:c.1670C= ENSP00000458312.1:n.1670C=
ENST00000572244.5:c.955C= ENSP00000461186.1:n.955C=
ENST00000574583.5:c.1037C= ENSP00000460269.1:n.1037C=
ENST00000576315.5:c.1070C= ENSP00000460551.1:n.1070C=
ENST00000621655.1:c.1802C= ENSP00000481436.1:n.1802C=
NM_000243.2:c.2265C= , LRG_190t1:c.2265C= NP_000234.1:p.Ile755=
NM_001198536.1:c.*469C= NP_001185465.1:n.*469C=
XM_017023236.2:c.2262C= XP_016878725.1:p.Ile754=
NM_000243.3:c.2265C= MANE Select NP_000234.1:p.Ile755=
NM_001198536.2:c.*469C= NP_001185465.2:n.*469C=