Canonical Allele Identifier: CA2202658545
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243224T= , CM000678.2:g.3243224T= GRCh38
NC_000016.9:g.3293224T= , CM000678.1:g.3293224T= GRCh37
NC_000016.8:g.3233225T= NCBI36
NG_007871.1:g.18404A= , LRG_190:g.18404A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1384A=
ENST00000219596.6:c.2263A= MANE Select ENSP00000219596.1:p.Ile755=
ENST00000219596.5:c.2263A= ENSP00000219596.1:p.Ile755=
ENST00000339854.8:c.1723A= ENSP00000339639.4:p.Ile575=
ENST00000536379.5:c.1630A= ENSP00000445079.1:p.Ile544=
ENST00000536980.5:c.*539A= ENSP00000444178.1:n.*539A=
ENST00000537682.5:c.*539A= ENSP00000438611.1:n.*539A=
ENST00000538326.5:c.*888A= ENSP00000437486.1:n.*888A=
ENST00000539145.5:c.1184A= ENSP00000444471.1:n.1184A=
ENST00000541159.5:c.1805A= ENSP00000438711.1:n.1805A=
ENST00000542898.5:c.*539A= ENSP00000444615.1:n.*539A=
ENST00000570511.5:c.1668A= ENSP00000458312.1:n.1668A=
ENST00000572244.5:c.953A= ENSP00000461186.1:n.953A=
ENST00000574583.5:c.1035A= ENSP00000460269.1:n.1035A=
ENST00000576315.5:c.1068A= ENSP00000460551.1:n.1068A=
ENST00000621655.1:c.1800A= ENSP00000481436.1:n.1800A=
NM_000243.2:c.2263A= , LRG_190t1:c.2263A= NP_000234.1:p.Ile755=
NM_001198536.1:c.*467A= NP_001185465.1:n.*467A=
XM_017023236.2:c.2260A= XP_016878725.1:p.Ile754=
NM_000243.3:c.2263A= MANE Select NP_000234.1:p.Ile755=
NM_001198536.2:c.*467A= NP_001185465.2:n.*467A=