Canonical Allele Identifier: CA2202658569
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243265T= , CM000678.2:g.3243265T= GRCh38
NC_000016.9:g.3293265T= , CM000678.1:g.3293265T= GRCh37
NC_000016.8:g.3233266T= NCBI36
NG_007871.1:g.18363A= , LRG_190:g.18363A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1343A=
ENST00000219596.6:c.2222A= MANE Select ENSP00000219596.1:p.Tyr741=
ENST00000219596.5:c.2222A= ENSP00000219596.1:p.Tyr741=
ENST00000339854.8:c.1682A= ENSP00000339639.4:p.Tyr561=
ENST00000536379.5:c.1589A= ENSP00000445079.1:p.Tyr530=
ENST00000536980.5:c.*498A= ENSP00000444178.1:n.*498A=
ENST00000537682.5:c.*498A= ENSP00000438611.1:n.*498A=
ENST00000538326.5:c.*847A= ENSP00000437486.1:n.*847A=
ENST00000539145.5:c.1143A= ENSP00000444471.1:n.1143A=
ENST00000541159.5:c.1764A= ENSP00000438711.1:n.1764A=
ENST00000542898.5:c.*498A= ENSP00000444615.1:n.*498A=
ENST00000570511.5:c.1627A= ENSP00000458312.1:n.1627A=
ENST00000572244.5:c.912A= ENSP00000461186.1:n.912A=
ENST00000574583.5:c.994A= ENSP00000460269.1:n.994A=
ENST00000576315.5:c.1027A= ENSP00000460551.1:n.1027A=
ENST00000621655.1:c.1759A= ENSP00000481436.1:n.1759A=
NM_000243.2:c.2222A= , LRG_190t1:c.2222A= NP_000234.1:p.Tyr741=
NM_001198536.1:c.*426A= NP_001185465.1:n.*426A=
XM_017023236.2:c.2219A= XP_016878725.1:p.Tyr740=
NM_000243.3:c.2222A= MANE Select NP_000234.1:p.Tyr741=
NM_001198536.2:c.*426A= NP_001185465.2:n.*426A=