Canonical Allele Identifier: CA394487832

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293586T>C (hg19) ; chr16:g.3243586T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243586T>C , CM000678.2:g.3243586T>C	GRCh38
NC_000016.9:g.3293586T>C , CM000678.1:g.3293586T>C	GRCh37
NC_000016.8:g.3233587T>C	NCBI36
NG_007871.1:g.18042A>G , LRG_190:g.18042A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1022A>G
ENST00000219596.6:c.1901A>G MANE Select	ENSP00000219596.1:p.Gln634Arg
ENST00000219596.5:c.1901A>G	ENSP00000219596.1:p.Gln634Arg
ENST00000339854.8:c.1361A>G	ENSP00000339639.4:p.Gln454Arg
ENST00000536379.5:c.1268A>G	ENSP00000445079.1:p.Gln423Arg
ENST00000536980.5:c.*177A>G	ENSP00000444178.1:n.*177A>G
ENST00000537682.5:c.*177A>G	ENSP00000438611.1:n.*177A>G
ENST00000538326.5:c.*526A>G	ENSP00000437486.1:n.*526A>G
ENST00000539145.5:c.822A>G	ENSP00000444471.1:n.822A>G
ENST00000541159.5:c.1443A>G	ENSP00000438711.1:n.1443A>G
ENST00000542898.5:c.*177A>G	ENSP00000444615.1:n.*177A>G
ENST00000570511.5:c.1306A>G	ENSP00000458312.1:n.1306A>G
ENST00000572244.5:c.591A>G	ENSP00000461186.1:n.591A>G
ENST00000574583.5:c.673A>G	ENSP00000460269.1:n.673A>G
ENST00000576315.5:c.706A>G	ENSP00000460551.1:n.706A>G
ENST00000621655.1:c.1438A>G	ENSP00000481436.1:n.1438A>G
NM_000243.2:c.1901A>G , LRG_190t1:c.1901A>G	NP_000234.1:p.Gln634Arg
NM_001198536.1:c.*105A>G	NP_001185465.1:n.*105A>G
XM_017023236.2:c.1898A>G	XP_016878725.1:p.Gln633Arg
NM_000243.3:c.1901A>G MANE Select	NP_000234.1:p.Gln634Arg
NM_001198536.2:c.*105A>G	NP_001185465.2:n.*105A>G