Canonical Allele Identifier: CA2202658674
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243451T= , CM000678.2:g.3243451T= GRCh38
NC_000016.9:g.3293451T= , CM000678.1:g.3293451T= GRCh37
NC_000016.8:g.3233452T= NCBI36
NG_007871.1:g.18177A= , LRG_190:g.18177A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1157A=
ENST00000219596.6:c.2036A= MANE Select ENSP00000219596.1:p.Asn679=
ENST00000219596.5:c.2036A= ENSP00000219596.1:p.Asn679=
ENST00000339854.8:c.1496A= ENSP00000339639.4:p.Asn499=
ENST00000536379.5:c.1403A= ENSP00000445079.1:p.Asn468=
ENST00000536980.5:c.*312A= ENSP00000444178.1:n.*312A=
ENST00000537682.5:c.*312A= ENSP00000438611.1:n.*312A=
ENST00000538326.5:c.*661A= ENSP00000437486.1:n.*661A=
ENST00000539145.5:c.957A= ENSP00000444471.1:n.957A=
ENST00000541159.5:c.1578A= ENSP00000438711.1:n.1578A=
ENST00000542898.5:c.*312A= ENSP00000444615.1:n.*312A=
ENST00000570511.5:c.1441A= ENSP00000458312.1:n.1441A=
ENST00000572244.5:c.726A= ENSP00000461186.1:n.726A=
ENST00000574583.5:c.808A= ENSP00000460269.1:n.808A=
ENST00000576315.5:c.841A= ENSP00000460551.1:n.841A=
ENST00000621655.1:c.1573A= ENSP00000481436.1:n.1573A=
NM_000243.2:c.2036A= , LRG_190t1:c.2036A= NP_000234.1:p.Asn679=
NM_001198536.1:c.*240A= NP_001185465.1:n.*240A=
XM_017023236.2:c.2033A= XP_016878725.1:p.Asn678=
NM_000243.3:c.2036A= MANE Select NP_000234.1:p.Asn679=
NM_001198536.2:c.*240A= NP_001185465.2:n.*240A=