Canonical Allele Identifier: CA2202658662
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243427C= , CM000678.2:g.3243427C= GRCh38
NC_000016.9:g.3293427C= , CM000678.1:g.3293427C= GRCh37
NC_000016.8:g.3233428C= NCBI36
NG_007871.1:g.18201G= , LRG_190:g.18201G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1181G=
ENST00000219596.6:c.2060G= MANE Select ENSP00000219596.1:p.Gly687=
ENST00000219596.5:c.2060G= ENSP00000219596.1:p.Gly687=
ENST00000339854.8:c.1520G= ENSP00000339639.4:p.Gly507=
ENST00000536379.5:c.1427G= ENSP00000445079.1:p.Gly476=
ENST00000536980.5:c.*336G= ENSP00000444178.1:n.*336G=
ENST00000537682.5:c.*336G= ENSP00000438611.1:n.*336G=
ENST00000538326.5:c.*685G= ENSP00000437486.1:n.*685G=
ENST00000539145.5:c.981G= ENSP00000444471.1:n.981G=
ENST00000541159.5:c.1602G= ENSP00000438711.1:n.1602G=
ENST00000542898.5:c.*336G= ENSP00000444615.1:n.*336G=
ENST00000570511.5:c.1465G= ENSP00000458312.1:n.1465G=
ENST00000572244.5:c.750G= ENSP00000461186.1:n.750G=
ENST00000574583.5:c.832G= ENSP00000460269.1:n.832G=
ENST00000576315.5:c.865G= ENSP00000460551.1:n.865G=
ENST00000621655.1:c.1597G= ENSP00000481436.1:n.1597G=
NM_000243.2:c.2060G= , LRG_190t1:c.2060G= NP_000234.1:p.Gly687=
NM_001198536.1:c.*264G= NP_001185465.1:n.*264G=
XM_017023236.2:c.2057G= XP_016878725.1:p.Gly686=
NM_000243.3:c.2060G= MANE Select NP_000234.1:p.Gly687=
NM_001198536.2:c.*264G= NP_001185465.2:n.*264G=