Canonical Allele Identifier: CA2202658920

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243934A= , CM000678.2:g.3243934A=	GRCh38
NC_000016.9:g.3293934A= , CM000678.1:g.3293934A=	GRCh37
NC_000016.8:g.3233935A=	NCBI36
NG_007871.1:g.17694T= , LRG_190:g.17694T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.881-42T=
ENST00000219596.6:c.1760-42T= MANE Select	ENSP00000219596.1:n.1760-42T=
ENST00000219596.5:c.1760-42T=	ENSP00000219596.1:n.1760-42T=
ENST00000339854.8:c.1220-42T=	ENSP00000339639.4:n.1220-42T=
ENST00000536379.5:c.1127-42T=	ENSP00000445079.1:n.1127-42T=
ENST00000536980.5:c.*36-42T=	ENSP00000444178.1:n.*36-42T=
ENST00000537682.5:c.*36-42T=	ENSP00000438611.1:n.*36-42T=
ENST00000538326.5:c.*385-42T=	ENSP00000437486.1:n.*385-42T=
ENST00000539145.5:c.681-42T=	ENSP00000444471.1:n.681-42T=
ENST00000541159.5:c.1260T=	ENSP00000438711.1:p.Ala420=
ENST00000542898.5:c.*36-42T=	ENSP00000444615.1:n.*36-42T=
ENST00000570511.5:c.1165-42T=	ENSP00000458312.1:n.1165-42T=
ENST00000572244.5:c.450-42T=	ENSP00000461186.1:n.450-42T=
ENST00000574583.5:c.532-42T=	ENSP00000460269.1:n.532-42T=
ENST00000576315.5:c.565-42T=	ENSP00000460551.1:n.565-42T=
ENST00000621655.1:c.1255T=	ENSP00000481436.1:n.1255T=
NM_000243.2:c.1760-42T= , LRG_190t1:c.1760-42T=	NP_000234.1:n.1760-42T=
NM_001198536.1:c.1260T=	NP_001185465.1:p.Ala420=
XM_017023236.2:c.1757-42T=	XP_016878725.1:n.1757-42T=
XR_001751903.1:n.2067-42T=
NM_000243.3:c.1760-42T= MANE Select	NP_000234.1:n.1760-42T=
NM_001198536.2:c.1260T=	NP_001185465.2:p.Ala420=