Canonical Allele Identifier: CA2202658349

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242865G= , CM000678.2:g.3242865G=	GRCh38
NC_000016.9:g.3292865G= , CM000678.1:g.3292865G=	GRCh37
NC_000016.8:g.3232866G=	NCBI36
NG_007871.1:g.18763C= , LRG_190:g.18763C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1743C=
ENST00000219596.6:c.*276C= MANE Select	ENSP00000219596.1:n.*276C=
ENST00000219596.5:c.*276C=	ENSP00000219596.1:n.*276C=
ENST00000339854.8:c.*276C=	ENSP00000339639.4:n.*276C=
ENST00000536980.5:c.*898C=	ENSP00000444178.1:n.*898C=
ENST00000537682.5:c.*898C=	ENSP00000438611.1:n.*898C=
ENST00000538326.5:c.*1247C=	ENSP00000437486.1:n.*1247C=
ENST00000542898.5:c.*898C=	ENSP00000444615.1:n.*898C=
NM_000243.2:c.*276C= , LRG_190t1:c.*276C=	NP_000234.1:n.*276C=
NM_001198536.1:c.*826C=	NP_001185465.1:n.*826C=
NM_000243.3:c.*276C= MANE Select	NP_000234.1:n.*276C=
NM_001198536.2:c.*826C=	NP_001185465.2:n.*826C=