Canonical Allele Identifier: CA493257617

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293168A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243168A>G , CM000678.2:g.3243168A>G	GRCh38
NC_000016.9:g.3293168A>G , CM000678.1:g.3293168A>G	GRCh37
NC_000016.8:g.3233169A>G	NCBI36
NG_007871.1:g.18460T>C , LRG_190:g.18460T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1440T>C
ENST00000219596.6:c.2319T>C MANE Select	ENSP00000219596.1:p.Cys773=
ENST00000219596.5:c.2319T>C	ENSP00000219596.1:p.Cys773=
ENST00000339854.8:c.1779T>C	ENSP00000339639.4:p.Cys593=
ENST00000536379.5:c.1686T>C	ENSP00000445079.1:p.Cys562=
ENST00000536980.5:c.*595T>C	ENSP00000444178.1:n.*595T>C
ENST00000537682.5:c.*595T>C	ENSP00000438611.1:n.*595T>C
ENST00000538326.5:c.*944T>C	ENSP00000437486.1:n.*944T>C
ENST00000539145.5:c.1240T>C	ENSP00000444471.1:n.1240T>C
ENST00000541159.5:c.1861T>C	ENSP00000438711.1:n.1861T>C
ENST00000542898.5:c.*595T>C	ENSP00000444615.1:n.*595T>C
ENST00000570511.5:c.1724T>C	ENSP00000458312.1:n.1724T>C
ENST00000572244.5:c.1009T>C	ENSP00000461186.1:n.1009T>C
ENST00000574583.5:c.1091T>C	ENSP00000460269.1:n.1091T>C
ENST00000576315.5:c.1124T>C	ENSP00000460551.1:n.1124T>C
ENST00000621655.1:c.1856T>C	ENSP00000481436.1:n.1856T>C
NM_000243.2:c.2319T>C , LRG_190t1:c.2319T>C	NP_000234.1:p.Cys773=
NM_001198536.1:c.*523T>C	NP_001185465.1:n.*523T>C
XM_017023236.2:c.2316T>C	XP_016878725.1:p.Cys772=
NM_000243.3:c.2319T>C MANE Select	NP_000234.1:p.Cys773=
NM_001198536.2:c.*523T>C	NP_001185465.2:n.*523T>C