Canonical Allele Identifier: CA2202658537

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243208G= , CM000678.2:g.3243208G=	GRCh38
NC_000016.9:g.3293208G= , CM000678.1:g.3293208G=	GRCh37
NC_000016.8:g.3233209G=	NCBI36
NG_007871.1:g.18420C= , LRG_190:g.18420C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1400C=
ENST00000219596.6:c.2279C= MANE Select	ENSP00000219596.1:p.Thr760=
ENST00000219596.5:c.2279C=	ENSP00000219596.1:p.Thr760=
ENST00000339854.8:c.1739C=	ENSP00000339639.4:p.Thr580=
ENST00000536379.5:c.1646C=	ENSP00000445079.1:p.Thr549=
ENST00000536980.5:c.*555C=	ENSP00000444178.1:n.*555C=
ENST00000537682.5:c.*555C=	ENSP00000438611.1:n.*555C=
ENST00000538326.5:c.*904C=	ENSP00000437486.1:n.*904C=
ENST00000539145.5:c.1200C=	ENSP00000444471.1:n.1200C=
ENST00000541159.5:c.1821C=	ENSP00000438711.1:n.1821C=
ENST00000542898.5:c.*555C=	ENSP00000444615.1:n.*555C=
ENST00000570511.5:c.1684C=	ENSP00000458312.1:n.1684C=
ENST00000572244.5:c.969C=	ENSP00000461186.1:n.969C=
ENST00000574583.5:c.1051C=	ENSP00000460269.1:n.1051C=
ENST00000576315.5:c.1084C=	ENSP00000460551.1:n.1084C=
ENST00000621655.1:c.1816C=	ENSP00000481436.1:n.1816C=
NM_000243.2:c.2279C= , LRG_190t1:c.2279C=	NP_000234.1:p.Thr760=
NM_001198536.1:c.*483C=	NP_001185465.1:n.*483C=
XM_017023236.2:c.2276C=	XP_016878725.1:p.Thr759=
NM_000243.3:c.2279C= MANE Select	NP_000234.1:p.Thr760=
NM_001198536.2:c.*483C=	NP_001185465.2:n.*483C=