Canonical Allele Identifier: CA2202658608

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243342G= , CM000678.2:g.3243342G=	GRCh38
NC_000016.9:g.3293342G= , CM000678.1:g.3293342G=	GRCh37
NC_000016.8:g.3233343G=	NCBI36
NG_007871.1:g.18286C= , LRG_190:g.18286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1266C=
ENST00000219596.6:c.2145C= MANE Select	ENSP00000219596.1:p.Pro715=
ENST00000219596.5:c.2145C=	ENSP00000219596.1:p.Pro715=
ENST00000339854.8:c.1605C=	ENSP00000339639.4:p.Pro535=
ENST00000536379.5:c.1512C=	ENSP00000445079.1:p.Pro504=
ENST00000536980.5:c.*421C=	ENSP00000444178.1:n.*421C=
ENST00000537682.5:c.*421C=	ENSP00000438611.1:n.*421C=
ENST00000538326.5:c.*770C=	ENSP00000437486.1:n.*770C=
ENST00000539145.5:c.1066C=	ENSP00000444471.1:n.1066C=
ENST00000541159.5:c.1687C=	ENSP00000438711.1:n.1687C=
ENST00000542898.5:c.*421C=	ENSP00000444615.1:n.*421C=
ENST00000570511.5:c.1550C=	ENSP00000458312.1:n.1550C=
ENST00000572244.5:c.835C=	ENSP00000461186.1:n.835C=
ENST00000574583.5:c.917C=	ENSP00000460269.1:n.917C=
ENST00000576315.5:c.950C=	ENSP00000460551.1:n.950C=
ENST00000621655.1:c.1682C=	ENSP00000481436.1:n.1682C=
NM_000243.2:c.2145C= , LRG_190t1:c.2145C=	NP_000234.1:p.Pro715=
NM_001198536.1:c.*349C=	NP_001185465.1:n.*349C=
XM_017023236.2:c.2142C=	XP_016878725.1:p.Pro714=
NM_000243.3:c.2145C= MANE Select	NP_000234.1:p.Pro715=
NM_001198536.2:c.*349C=	NP_001185465.2:n.*349C=