Canonical Allele Identifier: CA2202658390

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242930T= , CM000678.2:g.3242930T=	GRCh38
NC_000016.9:g.3292930T= , CM000678.1:g.3292930T=	GRCh37
NC_000016.8:g.3232931T=	NCBI36
NG_007871.1:g.18698A= , LRG_190:g.18698A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1678A=
ENST00000219596.6:c.*211A= MANE Select	ENSP00000219596.1:n.*211A=
ENST00000219596.5:c.*211A=	ENSP00000219596.1:n.*211A=
ENST00000339854.8:c.*211A=	ENSP00000339639.4:n.*211A=
ENST00000536980.5:c.*833A=	ENSP00000444178.1:n.*833A=
ENST00000537682.5:c.*833A=	ENSP00000438611.1:n.*833A=
ENST00000538326.5:c.*1182A=	ENSP00000437486.1:n.*1182A=
ENST00000542898.5:c.*833A=	ENSP00000444615.1:n.*833A=
NM_000243.2:c.*211A= , LRG_190t1:c.*211A=	NP_000234.1:n.*211A=
NM_001198536.1:c.*761A=	NP_001185465.1:n.*761A=
NM_000243.3:c.*211A= MANE Select	NP_000234.1:n.*211A=
NM_001198536.2:c.*761A=	NP_001185465.2:n.*761A=