Canonical Allele Identifier: CA394485895

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293371G>T (hg19) ; chr16:g.3243371G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243371G>T , CM000678.2:g.3243371G>T	GRCh38
NC_000016.9:g.3293371G>T , CM000678.1:g.3293371G>T	GRCh37
NC_000016.8:g.3233372G>T	NCBI36
NG_007871.1:g.18257C>A , LRG_190:g.18257C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1237C>A
ENST00000219596.6:c.2116C>A MANE Select	ENSP00000219596.1:p.Pro706Thr
ENST00000219596.5:c.2116C>A	ENSP00000219596.1:p.Pro706Thr
ENST00000339854.8:c.1576C>A	ENSP00000339639.4:p.Pro526Thr
ENST00000536379.5:c.1483C>A	ENSP00000445079.1:p.Pro495Thr
ENST00000536980.5:c.*392C>A	ENSP00000444178.1:n.*392C>A
ENST00000537682.5:c.*392C>A	ENSP00000438611.1:n.*392C>A
ENST00000538326.5:c.*741C>A	ENSP00000437486.1:n.*741C>A
ENST00000539145.5:c.1037C>A	ENSP00000444471.1:n.1037C>A
ENST00000541159.5:c.1658C>A	ENSP00000438711.1:n.1658C>A
ENST00000542898.5:c.*392C>A	ENSP00000444615.1:n.*392C>A
ENST00000570511.5:c.1521C>A	ENSP00000458312.1:n.1521C>A
ENST00000572244.5:c.806C>A	ENSP00000461186.1:n.806C>A
ENST00000574583.5:c.888C>A	ENSP00000460269.1:n.888C>A
ENST00000576315.5:c.921C>A	ENSP00000460551.1:n.921C>A
ENST00000621655.1:c.1653C>A	ENSP00000481436.1:n.1653C>A
NM_000243.2:c.2116C>A , LRG_190t1:c.2116C>A	NP_000234.1:p.Pro706Thr
NM_001198536.1:c.*320C>A	NP_001185465.1:n.*320C>A
XM_017023236.2:c.2113C>A	XP_016878725.1:p.Pro705Thr
NM_000243.3:c.2116C>A MANE Select	NP_000234.1:p.Pro706Thr
NM_001198536.2:c.*320C>A	NP_001185465.2:n.*320C>A