Canonical Allele Identifier: CA2202658604
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243337C= , CM000678.2:g.3243337C= GRCh38
NC_000016.9:g.3293337C= , CM000678.1:g.3293337C= GRCh37
NC_000016.8:g.3233338C= NCBI36
NG_007871.1:g.18291G= , LRG_190:g.18291G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1271G=
ENST00000219596.6:c.2150G= MANE Select ENSP00000219596.1:p.Arg717=
ENST00000219596.5:c.2150G= ENSP00000219596.1:p.Arg717=
ENST00000339854.8:c.1610G= ENSP00000339639.4:p.Arg537=
ENST00000536379.5:c.1517G= ENSP00000445079.1:p.Arg506=
ENST00000536980.5:c.*426G= ENSP00000444178.1:n.*426G=
ENST00000537682.5:c.*426G= ENSP00000438611.1:n.*426G=
ENST00000538326.5:c.*775G= ENSP00000437486.1:n.*775G=
ENST00000539145.5:c.1071G= ENSP00000444471.1:n.1071G=
ENST00000541159.5:c.1692G= ENSP00000438711.1:n.1692G=
ENST00000542898.5:c.*426G= ENSP00000444615.1:n.*426G=
ENST00000570511.5:c.1555G= ENSP00000458312.1:n.1555G=
ENST00000572244.5:c.840G= ENSP00000461186.1:n.840G=
ENST00000574583.5:c.922G= ENSP00000460269.1:n.922G=
ENST00000576315.5:c.955G= ENSP00000460551.1:n.955G=
ENST00000621655.1:c.1687G= ENSP00000481436.1:n.1687G=
NM_000243.2:c.2150G= , LRG_190t1:c.2150G= NP_000234.1:p.Arg717=
NM_001198536.1:c.*354G= NP_001185465.1:n.*354G=
XM_017023236.2:c.2147G= XP_016878725.1:p.Arg716=
NM_000243.3:c.2150G= MANE Select NP_000234.1:p.Arg717=
NM_001198536.2:c.*354G= NP_001185465.2:n.*354G=