Canonical Allele Identifier: CA2202658494

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243128C= , CM000678.2:g.3243128C=	GRCh38
NC_000016.9:g.3293128C= , CM000678.1:g.3293128C=	GRCh37
NC_000016.8:g.3233129C=	NCBI36
NG_007871.1:g.18500G= , LRG_190:g.18500G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1480G=
ENST00000219596.6:c.*13G= MANE Select	ENSP00000219596.1:n.*13G=
ENST00000219596.5:c.*13G=	ENSP00000219596.1:n.*13G=
ENST00000339854.8:c.*13G=	ENSP00000339639.4:n.*13G=
ENST00000536980.5:c.*635G=	ENSP00000444178.1:n.*635G=
ENST00000537682.5:c.*635G=	ENSP00000438611.1:n.*635G=
ENST00000538326.5:c.*984G=	ENSP00000437486.1:n.*984G=
ENST00000542898.5:c.*635G=	ENSP00000444615.1:n.*635G=
NM_000243.2:c.*13G= , LRG_190t1:c.*13G=	NP_000234.1:n.*13G=
NM_001198536.1:c.*563G=	NP_001185465.1:n.*563G=
XM_017023236.2:c.*13G=	XP_016878725.1:n.*13G=
NM_000243.3:c.*13G= MANE Select	NP_000234.1:n.*13G=
NM_001198536.2:c.*563G=	NP_001185465.2:n.*563G=