Canonical Allele Identifier: CA394463663

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3297091C>A (hg19) ; chr16:g.3247091C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247091C>A , CM000678.2:g.3247091C>A	GRCh38
NC_000016.9:g.3297091C>A , CM000678.1:g.3297091C>A	GRCh37
NC_000016.8:g.3237092C>A	NCBI36
NG_007871.1:g.14537G>T , LRG_190:g.14537G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.1512G>T MANE Select	ENSP00000219596.1:p.Gln504His
ENST00000219596.5:c.1512G>T	ENSP00000219596.1:p.Gln504His
ENST00000339854.8:c.972G>T	ENSP00000339639.4:p.Gln324His
ENST00000536379.5:c.879G>T	ENSP00000445079.1:p.Gln293His
ENST00000536980.5:c.879G>T	ENSP00000444178.1:p.Gln293His
ENST00000537682.5:c.1512G>T	ENSP00000438611.1:p.Gln504His
ENST00000538326.5:c.*137G>T	ENSP00000437486.1:n.*137G>T
ENST00000539145.5:c.433G>T	ENSP00000444471.1:n.433G>T
ENST00000539154.1:n.877G>T
ENST00000541159.5:c.879G>T	ENSP00000438711.1:p.Gln293His
ENST00000542898.5:c.1605G>T	ENSP00000444615.1:p.Gln535His
ENST00000570511.5:c.1066G>T	ENSP00000458312.1:n.1066G>T
ENST00000572244.5:c.278-544G>T	ENSP00000461186.1:n.278-544G>T
ENST00000574583.5:c.433G>T	ENSP00000460269.1:n.433G>T
ENST00000576315.5:c.433G>T	ENSP00000460551.1:n.433G>T
ENST00000621655.1:c.879G>T	ENSP00000481436.1:p.Gln293His
NM_000243.2:c.1512G>T , LRG_190t1:c.1512G>T	NP_000234.1:p.Gln504His
NM_001198536.1:c.879G>T	NP_001185465.1:p.Gln293His
XM_017023236.2:c.1509G>T	XP_016878725.1:p.Gln503His
XR_001751903.1:n.1701G>T
NM_000243.3:c.1512G>T MANE Select	NP_000234.1:p.Gln504His
NM_001198536.2:c.879G>T	NP_001185465.2:p.Gln293His