Canonical Allele Identifier: CA2202658394

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242935T= , CM000678.2:g.3242935T=	GRCh38
NC_000016.9:g.3292935T= , CM000678.1:g.3292935T=	GRCh37
NC_000016.8:g.3232936T=	NCBI36
NG_007871.1:g.18693A= , LRG_190:g.18693A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1673A=
ENST00000219596.6:c.*206A= MANE Select	ENSP00000219596.1:n.*206A=
ENST00000219596.5:c.*206A=	ENSP00000219596.1:n.*206A=
ENST00000339854.8:c.*206A=	ENSP00000339639.4:n.*206A=
ENST00000536980.5:c.*828A=	ENSP00000444178.1:n.*828A=
ENST00000537682.5:c.*828A=	ENSP00000438611.1:n.*828A=
ENST00000538326.5:c.*1177A=	ENSP00000437486.1:n.*1177A=
ENST00000542898.5:c.*828A=	ENSP00000444615.1:n.*828A=
NM_000243.2:c.*206A= , LRG_190t1:c.*206A=	NP_000234.1:n.*206A=
NM_001198536.1:c.*756A=	NP_001185465.1:n.*756A=
NM_000243.3:c.*206A= MANE Select	NP_000234.1:n.*206A=
NM_001198536.2:c.*756A=	NP_001185465.2:n.*756A=