Canonical Allele Identifier: CA2202660634

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247158G= , CM000678.2:g.3247158G=	GRCh38
NC_000016.9:g.3297158G= , CM000678.1:g.3297158G=	GRCh37
NC_000016.8:g.3237159G=	NCBI36
NG_007871.1:g.14470C= , LRG_190:g.14470C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.1445C= MANE Select	ENSP00000219596.1:p.Ala482=
ENST00000219596.5:c.1445C=	ENSP00000219596.1:p.Ala482=
ENST00000339854.8:c.905C=	ENSP00000339639.4:p.Ala302=
ENST00000536379.5:c.812C=	ENSP00000445079.1:p.Ala271=
ENST00000536980.5:c.812C=	ENSP00000444178.1:p.Ala271=
ENST00000537682.5:c.1445C=	ENSP00000438611.1:p.Ala482=
ENST00000538326.5:c.*70C=	ENSP00000437486.1:n.*70C=
ENST00000539145.5:c.366C=	ENSP00000444471.1:n.366C=
ENST00000539154.1:n.810C=
ENST00000541159.5:c.812C=	ENSP00000438711.1:p.Ala271=
ENST00000542898.5:c.1538C=	ENSP00000444615.1:p.Ala513=
ENST00000570511.5:c.999C=	ENSP00000458312.1:n.999C=
ENST00000572244.5:c.278-611C=	ENSP00000461186.1:n.278-611C=
ENST00000574583.5:c.366C=	ENSP00000460269.1:n.366C=
ENST00000576315.5:c.366C=	ENSP00000460551.1:n.366C=
ENST00000621655.1:c.812C=	ENSP00000481436.1:p.Ala271=
NM_000243.2:c.1445C= , LRG_190t1:c.1445C=	NP_000234.1:p.Ala482=
NM_001198536.1:c.812C=	NP_001185465.1:p.Ala271=
XM_017023236.2:c.1442C=	XP_016878725.1:p.Ala481=
XR_001751903.1:n.1634C=
NM_000243.3:c.1445C= MANE Select	NP_000234.1:p.Ala482=
NM_001198536.2:c.812C=	NP_001185465.2:p.Ala271=