Canonical Allele Identifier: CA2202658877

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243870C= , CM000678.2:g.3243870C=	GRCh38
NC_000016.9:g.3293870C= , CM000678.1:g.3293870C=	GRCh37
NC_000016.8:g.3233871C=	NCBI36
NG_007871.1:g.17758G= , LRG_190:g.17758G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.903G=
ENST00000219596.6:c.1782G= MANE Select	ENSP00000219596.1:p.Gln594=
ENST00000219596.5:c.1782G=	ENSP00000219596.1:p.Gln594=
ENST00000339854.8:c.1242G=	ENSP00000339639.4:p.Gln414=
ENST00000536379.5:c.1149G=	ENSP00000445079.1:p.Gln383=
ENST00000536980.5:c.*58G=	ENSP00000444178.1:n.*58G=
ENST00000537682.5:c.*58G=	ENSP00000438611.1:n.*58G=
ENST00000538326.5:c.*407G=	ENSP00000437486.1:n.*407G=
ENST00000539145.5:c.703G=	ENSP00000444471.1:n.703G=
ENST00000541159.5:c.1324G=	ENSP00000438711.1:p.Gly442=
ENST00000542898.5:c.*58G=	ENSP00000444615.1:n.*58G=
ENST00000570511.5:c.1187G=	ENSP00000458312.1:n.1187G=
ENST00000572244.5:c.472G=	ENSP00000461186.1:n.472G=
ENST00000574583.5:c.554G=	ENSP00000460269.1:n.554G=
ENST00000576315.5:c.587G=	ENSP00000460551.1:n.587G=
ENST00000621655.1:c.1319G=	ENSP00000481436.1:n.1319G=
NM_000243.2:c.1782G= , LRG_190t1:c.1782G=	NP_000234.1:p.Gln594=
NM_001198536.1:c.1324G=	NP_001185465.1:p.Gly442=
XM_017023236.2:c.1779G=	XP_016878725.1:p.Gln593=
XR_001751903.1:n.2089G=
NM_000243.3:c.1782G= MANE Select	NP_000234.1:p.Gln594=
NM_001198536.2:c.1324G=	NP_001185465.2:p.Gly442=