Canonical Allele Identifier: CA2202658558
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243253C= , CM000678.2:g.3243253C= GRCh38
NC_000016.9:g.3293253C= , CM000678.1:g.3293253C= GRCh37
NC_000016.8:g.3233254C= NCBI36
NG_007871.1:g.18375G= , LRG_190:g.18375G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1355G=
ENST00000219596.6:c.2234G= MANE Select ENSP00000219596.1:p.Ser745=
ENST00000219596.5:c.2234G= ENSP00000219596.1:p.Ser745=
ENST00000339854.8:c.1694G= ENSP00000339639.4:p.Ser565=
ENST00000536379.5:c.1601G= ENSP00000445079.1:p.Ser534=
ENST00000536980.5:c.*510G= ENSP00000444178.1:n.*510G=
ENST00000537682.5:c.*510G= ENSP00000438611.1:n.*510G=
ENST00000538326.5:c.*859G= ENSP00000437486.1:n.*859G=
ENST00000539145.5:c.1155G= ENSP00000444471.1:n.1155G=
ENST00000541159.5:c.1776G= ENSP00000438711.1:n.1776G=
ENST00000542898.5:c.*510G= ENSP00000444615.1:n.*510G=
ENST00000570511.5:c.1639G= ENSP00000458312.1:n.1639G=
ENST00000572244.5:c.924G= ENSP00000461186.1:n.924G=
ENST00000574583.5:c.1006G= ENSP00000460269.1:n.1006G=
ENST00000576315.5:c.1039G= ENSP00000460551.1:n.1039G=
ENST00000621655.1:c.1771G= ENSP00000481436.1:n.1771G=
NM_000243.2:c.2234G= , LRG_190t1:c.2234G= NP_000234.1:p.Ser745=
NM_001198536.1:c.*438G= NP_001185465.1:n.*438G=
XM_017023236.2:c.2231G= XP_016878725.1:p.Ser744=
NM_000243.3:c.2234G= MANE Select NP_000234.1:p.Ser745=
NM_001198536.2:c.*438G= NP_001185465.2:n.*438G=