Canonical Allele Identifier: CA2202658871

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243860C= , CM000678.2:g.3243860C=	GRCh38
NC_000016.9:g.3293860C= , CM000678.1:g.3293860C=	GRCh37
NC_000016.8:g.3233861C=	NCBI36
NG_007871.1:g.17768G= , LRG_190:g.17768G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.913G=
ENST00000219596.6:c.1792G= MANE Select	ENSP00000219596.1:p.Val598=
ENST00000219596.5:c.1792G=	ENSP00000219596.1:p.Val598=
ENST00000339854.8:c.1252G=	ENSP00000339639.4:p.Val418=
ENST00000536379.5:c.1159G=	ENSP00000445079.1:p.Val387=
ENST00000536980.5:c.*68G=	ENSP00000444178.1:n.*68G=
ENST00000537682.5:c.*68G=	ENSP00000438611.1:n.*68G=
ENST00000538326.5:c.*417G=	ENSP00000437486.1:n.*417G=
ENST00000539145.5:c.713G=	ENSP00000444471.1:n.713G=
ENST00000541159.5:c.1334G=	ENSP00000438711.1:p.Cys445=
ENST00000542898.5:c.*68G=	ENSP00000444615.1:n.*68G=
ENST00000570511.5:c.1197G=	ENSP00000458312.1:n.1197G=
ENST00000572244.5:c.482G=	ENSP00000461186.1:n.482G=
ENST00000574583.5:c.564G=	ENSP00000460269.1:n.564G=
ENST00000576315.5:c.597G=	ENSP00000460551.1:n.597G=
ENST00000621655.1:c.1329G=	ENSP00000481436.1:n.1329G=
NM_000243.2:c.1792G= , LRG_190t1:c.1792G=	NP_000234.1:p.Val598=
NM_001198536.1:c.1334G=	NP_001185465.1:p.Cys445=
XM_017023236.2:c.1789G=	XP_016878725.1:p.Val597=
XR_001751903.1:n.2099G=
NM_000243.3:c.1792G= MANE Select	NP_000234.1:p.Val598=
NM_001198536.2:c.1334G=	NP_001185465.2:p.Cys445=