Canonical Allele Identifier: CA2202658679
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243461T= , CM000678.2:g.3243461T= GRCh38
NC_000016.9:g.3293461T= , CM000678.1:g.3293461T= GRCh37
NC_000016.8:g.3233462T= NCBI36
NG_007871.1:g.18167A= , LRG_190:g.18167A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1147A=
ENST00000219596.6:c.2026A= MANE Select ENSP00000219596.1:p.Arg676=
ENST00000219596.5:c.2026A= ENSP00000219596.1:p.Arg676=
ENST00000339854.8:c.1486A= ENSP00000339639.4:p.Arg496=
ENST00000536379.5:c.1393A= ENSP00000445079.1:p.Arg465=
ENST00000536980.5:c.*302A= ENSP00000444178.1:n.*302A=
ENST00000537682.5:c.*302A= ENSP00000438611.1:n.*302A=
ENST00000538326.5:c.*651A= ENSP00000437486.1:n.*651A=
ENST00000539145.5:c.947A= ENSP00000444471.1:n.947A=
ENST00000541159.5:c.1568A= ENSP00000438711.1:n.1568A=
ENST00000542898.5:c.*302A= ENSP00000444615.1:n.*302A=
ENST00000570511.5:c.1431A= ENSP00000458312.1:n.1431A=
ENST00000572244.5:c.716A= ENSP00000461186.1:n.716A=
ENST00000574583.5:c.798A= ENSP00000460269.1:n.798A=
ENST00000576315.5:c.831A= ENSP00000460551.1:n.831A=
ENST00000621655.1:c.1563A= ENSP00000481436.1:n.1563A=
NM_000243.2:c.2026A= , LRG_190t1:c.2026A= NP_000234.1:p.Arg676=
NM_001198536.1:c.*230A= NP_001185465.1:n.*230A=
XM_017023236.2:c.2023A= XP_016878725.1:p.Arg675=
NM_000243.3:c.2026A= MANE Select NP_000234.1:p.Arg676=
NM_001198536.2:c.*230A= NP_001185465.2:n.*230A=