Canonical Allele Identifier: CA2202658441

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243027T= , CM000678.2:g.3243027T=	GRCh38
NC_000016.9:g.3293027T= , CM000678.1:g.3293027T=	GRCh37
NC_000016.8:g.3233028T=	NCBI36
NG_007871.1:g.18601A= , LRG_190:g.18601A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1581A=
ENST00000219596.6:c.*114A= MANE Select	ENSP00000219596.1:n.*114A=
ENST00000219596.5:c.*114A=	ENSP00000219596.1:n.*114A=
ENST00000339854.8:c.*114A=	ENSP00000339639.4:n.*114A=
ENST00000536980.5:c.*736A=	ENSP00000444178.1:n.*736A=
ENST00000537682.5:c.*736A=	ENSP00000438611.1:n.*736A=
ENST00000538326.5:c.*1085A=	ENSP00000437486.1:n.*1085A=
ENST00000542898.5:c.*736A=	ENSP00000444615.1:n.*736A=
NM_000243.2:c.*114A= , LRG_190t1:c.*114A=	NP_000234.1:n.*114A=
NM_001198536.1:c.*664A=	NP_001185465.1:n.*664A=
NM_000243.3:c.*114A= MANE Select	NP_000234.1:n.*114A=
NM_001198536.2:c.*664A=	NP_001185465.2:n.*664A=