Canonical Allele Identifier: CA2202658408

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242964A= , CM000678.2:g.3242964A=	GRCh38
NC_000016.9:g.3292964A= , CM000678.1:g.3292964A=	GRCh37
NC_000016.8:g.3232965A=	NCBI36
NG_007871.1:g.18664T= , LRG_190:g.18664T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1644T=
ENST00000219596.6:c.*177T= MANE Select	ENSP00000219596.1:n.*177T=
ENST00000219596.5:c.*177T=	ENSP00000219596.1:n.*177T=
ENST00000339854.8:c.*177T=	ENSP00000339639.4:n.*177T=
ENST00000536980.5:c.*799T=	ENSP00000444178.1:n.*799T=
ENST00000537682.5:c.*799T=	ENSP00000438611.1:n.*799T=
ENST00000538326.5:c.*1148T=	ENSP00000437486.1:n.*1148T=
ENST00000542898.5:c.*799T=	ENSP00000444615.1:n.*799T=
NM_000243.2:c.*177T= , LRG_190t1:c.*177T=	NP_000234.1:n.*177T=
NM_001198536.1:c.*727T=	NP_001185465.1:n.*727T=
NM_000243.3:c.*177T= MANE Select	NP_000234.1:n.*177T=
NM_001198536.2:c.*727T=	NP_001185465.2:n.*727T=