Canonical Allele Identifier: CA493383607

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293291G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243291G>A , CM000678.2:g.3243291G>A	GRCh38
NC_000016.9:g.3293291G>A , CM000678.1:g.3293291G>A	GRCh37
NC_000016.8:g.3233292G>A	NCBI36
NG_007871.1:g.18337C>T , LRG_190:g.18337C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1317C>T
ENST00000219596.6:c.2196C>T MANE Select	ENSP00000219596.1:p.Tyr732=
ENST00000219596.5:c.2196C>T	ENSP00000219596.1:p.Tyr732=
ENST00000339854.8:c.1656C>T	ENSP00000339639.4:p.Tyr552=
ENST00000536379.5:c.1563C>T	ENSP00000445079.1:p.Tyr521=
ENST00000536980.5:c.*472C>T	ENSP00000444178.1:n.*472C>T
ENST00000537682.5:c.*472C>T	ENSP00000438611.1:n.*472C>T
ENST00000538326.5:c.*821C>T	ENSP00000437486.1:n.*821C>T
ENST00000539145.5:c.1117C>T	ENSP00000444471.1:n.1117C>T
ENST00000541159.5:c.1738C>T	ENSP00000438711.1:n.1738C>T
ENST00000542898.5:c.*472C>T	ENSP00000444615.1:n.*472C>T
ENST00000570511.5:c.1601C>T	ENSP00000458312.1:n.1601C>T
ENST00000572244.5:c.886C>T	ENSP00000461186.1:n.886C>T
ENST00000574583.5:c.968C>T	ENSP00000460269.1:n.968C>T
ENST00000576315.5:c.1001C>T	ENSP00000460551.1:n.1001C>T
ENST00000621655.1:c.1733C>T	ENSP00000481436.1:n.1733C>T
NM_000243.2:c.2196C>T , LRG_190t1:c.2196C>T	NP_000234.1:p.Tyr732=
NM_001198536.1:c.*400C>T	NP_001185465.1:n.*400C>T
XM_017023236.2:c.2193C>T	XP_016878725.1:p.Tyr731=
NM_000243.3:c.2196C>T MANE Select	NP_000234.1:p.Tyr732=
NM_001198536.2:c.*400C>T	NP_001185465.2:n.*400C>T