Canonical Allele Identifier: CA2202660640

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247166G= , CM000678.2:g.3247166G=	GRCh38
NC_000016.9:g.3297166G= , CM000678.1:g.3297166G=	GRCh37
NC_000016.8:g.3237167G=	NCBI36
NG_007871.1:g.14462C= , LRG_190:g.14462C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000243.3:c.1437C= MANE Select	NP_000234.1:p.Phe479=
ENST00000219596.6:c.1437C= MANE Select	ENSP00000219596.1:p.Phe479=
NM_000243.2:c.1437C= , LRG_190t1:c.1437C=	NP_000234.1:p.Phe479=
NM_001198536.1:c.804C=	NP_001185465.1:p.Phe268=
NM_001198536.2:c.804C=	NP_001185465.2:p.Phe268=
ENST00000219596.5:c.1437C=	ENSP00000219596.1:p.Phe479=
ENST00000339854.8:c.897C=	ENSP00000339639.4:p.Phe299=
ENST00000536379.5:c.804C=	ENSP00000445079.1:p.Phe268=
ENST00000536980.5:c.804C=	ENSP00000444178.1:p.Phe268=
ENST00000537682.5:c.1437C=	ENSP00000438611.1:p.Phe479=
ENST00000538326.5:c.*62C=	ENSP00000437486.1:n.*62C=
ENST00000539145.5:c.358C=	ENSP00000444471.1:n.358C=
ENST00000539154.1:n.802C=
ENST00000541159.5:c.804C=	ENSP00000438711.1:p.Phe268=
ENST00000542898.5:c.1530C=	ENSP00000444615.1:p.Phe510=
ENST00000570511.5:c.991C=	ENSP00000458312.1:n.991C=
ENST00000572244.5:c.278-619C=	ENSP00000461186.1:n.278-619C=
ENST00000574583.5:c.358C=	ENSP00000460269.1:n.358C=
ENST00000576315.5:c.358C=	ENSP00000460551.1:n.358C=
ENST00000621655.1:c.804C=	ENSP00000481436.1:p.Phe268=
XM_017023236.2:c.1434C=	XP_016878725.1:p.Phe478=
XR_001751903.1:n.1626C=