Canonical Allele Identifier: CA2202666006

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3256600G= , CM000678.2:g.3256600G=	GRCh38
NC_000016.9:g.3306600G= , CM000678.1:g.3306600G=	GRCh37
NC_000016.8:g.3246601G=	NCBI36
NG_007871.1:g.5028C= , LRG_190:g.5028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.-13C= MANE Select	ENSP00000219596.1:n.-13C=
ENST00000219596.5:c.-13C=	ENSP00000219596.1:n.-13C=
ENST00000339854.8:c.-13C=	ENSP00000339639.4:n.-13C=
ENST00000536980.5:c.-13C=	ENSP00000444178.1:n.-13C=
ENST00000537682.5:c.-13C=	ENSP00000438611.1:n.-13C=
ENST00000538326.5:c.-13C=	ENSP00000437486.1:n.-13C=
ENST00000542898.5:c.-13C=	ENSP00000444615.1:n.-13C=
NM_000243.2:c.-13C= , LRG_190t1:c.-13C=	NP_000234.1:n.-13C=
NM_001198536.1:c.-13C=	NP_001185465.1:n.-13C=
XM_017023236.2:c.-13C=	XP_016878725.1:n.-13C=
XR_001751903.1:n.177C=
NM_000243.3:c.-13C= MANE Select	NP_000234.1:n.-13C=
NM_001198536.2:c.-13C=	NP_001185465.2:n.-13C=