Canonical Allele Identifier: CA2202658640

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243391T= , CM000678.2:g.3243391T=	GRCh38
NC_000016.9:g.3293391T= , CM000678.1:g.3293391T=	GRCh37
NC_000016.8:g.3233392T=	NCBI36
NG_007871.1:g.18237A= , LRG_190:g.18237A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1217A=
ENST00000219596.6:c.2096A= MANE Select	ENSP00000219596.1:p.Tyr699=
ENST00000219596.5:c.2096A=	ENSP00000219596.1:p.Tyr699=
ENST00000339854.8:c.1556A=	ENSP00000339639.4:p.Tyr519=
ENST00000536379.5:c.1463A=	ENSP00000445079.1:p.Tyr488=
ENST00000536980.5:c.*372A=	ENSP00000444178.1:n.*372A=
ENST00000537682.5:c.*372A=	ENSP00000438611.1:n.*372A=
ENST00000538326.5:c.*721A=	ENSP00000437486.1:n.*721A=
ENST00000539145.5:c.1017A=	ENSP00000444471.1:n.1017A=
ENST00000541159.5:c.1638A=	ENSP00000438711.1:n.1638A=
ENST00000542898.5:c.*372A=	ENSP00000444615.1:n.*372A=
ENST00000570511.5:c.1501A=	ENSP00000458312.1:n.1501A=
ENST00000572244.5:c.786A=	ENSP00000461186.1:n.786A=
ENST00000574583.5:c.868A=	ENSP00000460269.1:n.868A=
ENST00000576315.5:c.901A=	ENSP00000460551.1:n.901A=
ENST00000621655.1:c.1633A=	ENSP00000481436.1:n.1633A=
NM_000243.2:c.2096A= , LRG_190t1:c.2096A=	NP_000234.1:p.Tyr699=
NM_001198536.1:c.*300A=	NP_001185465.1:n.*300A=
XM_017023236.2:c.2093A=	XP_016878725.1:p.Tyr698=
NM_000243.3:c.2096A= MANE Select	NP_000234.1:p.Tyr699=
NM_001198536.2:c.*300A=	NP_001185465.2:n.*300A=