Canonical Allele Identifier: CA2202658549
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243235G= , CM000678.2:g.3243235G= GRCh38
NC_000016.9:g.3293235G= , CM000678.1:g.3293235G= GRCh37
NC_000016.8:g.3233236G= NCBI36
NG_007871.1:g.18393C= , LRG_190:g.18393C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1373C=
ENST00000219596.6:c.2252C= MANE Select ENSP00000219596.1:p.Pro751=
ENST00000219596.5:c.2252C= ENSP00000219596.1:p.Pro751=
ENST00000339854.8:c.1712C= ENSP00000339639.4:p.Pro571=
ENST00000536379.5:c.1619C= ENSP00000445079.1:p.Pro540=
ENST00000536980.5:c.*528C= ENSP00000444178.1:n.*528C=
ENST00000537682.5:c.*528C= ENSP00000438611.1:n.*528C=
ENST00000538326.5:c.*877C= ENSP00000437486.1:n.*877C=
ENST00000539145.5:c.1173C= ENSP00000444471.1:n.1173C=
ENST00000541159.5:c.1794C= ENSP00000438711.1:n.1794C=
ENST00000542898.5:c.*528C= ENSP00000444615.1:n.*528C=
ENST00000570511.5:c.1657C= ENSP00000458312.1:n.1657C=
ENST00000572244.5:c.942C= ENSP00000461186.1:n.942C=
ENST00000574583.5:c.1024C= ENSP00000460269.1:n.1024C=
ENST00000576315.5:c.1057C= ENSP00000460551.1:n.1057C=
ENST00000621655.1:c.1789C= ENSP00000481436.1:n.1789C=
NM_000243.2:c.2252C= , LRG_190t1:c.2252C= NP_000234.1:p.Pro751=
NM_001198536.1:c.*456C= NP_001185465.1:n.*456C=
XM_017023236.2:c.2249C= XP_016878725.1:p.Pro750=
NM_000243.3:c.2252C= MANE Select NP_000234.1:p.Pro751=
NM_001198536.2:c.*456C= NP_001185465.2:n.*456C=