Canonical Allele Identifier: CA394488997

Gene: MEFV

Linked Data

• ClinVar Variation Id: 2114201
• ClinVar RCV Id: RCV003042668
• MyVariant Identifiers: chr16:g.3293893C>A (hg19) ; chr16:g.3243893C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243893C>A , CM000678.2:g.3243893C>A	GRCh38
NC_000016.9:g.3293893C>A , CM000678.1:g.3293893C>A	GRCh37
NC_000016.8:g.3233894C>A	NCBI36
NG_007871.1:g.17735G>T , LRG_190:g.17735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.881-1G>T
ENST00000219596.6:c.1760-1G>T MANE Select	ENSP00000219596.1:n.1760-1G>T
ENST00000219596.5:c.1760-1G>T	ENSP00000219596.1:n.1760-1G>T
ENST00000339854.8:c.1220-1G>T	ENSP00000339639.4:n.1220-1G>T
ENST00000536379.5:c.1127-1G>T	ENSP00000445079.1:n.1127-1G>T
ENST00000536980.5:c.*36-1G>T	ENSP00000444178.1:n.*36-1G>T
ENST00000537682.5:c.*36-1G>T	ENSP00000438611.1:n.*36-1G>T
ENST00000538326.5:c.*385-1G>T	ENSP00000437486.1:n.*385-1G>T
ENST00000539145.5:c.681-1G>T	ENSP00000444471.1:n.681-1G>T
ENST00000541159.5:c.1301G>T	ENSP00000438711.1:p.Ser434Ile
ENST00000542898.5:c.*36-1G>T	ENSP00000444615.1:n.*36-1G>T
ENST00000570511.5:c.1165-1G>T	ENSP00000458312.1:n.1165-1G>T
ENST00000572244.5:c.450-1G>T	ENSP00000461186.1:n.450-1G>T
ENST00000574583.5:c.532-1G>T	ENSP00000460269.1:n.532-1G>T
ENST00000576315.5:c.565-1G>T	ENSP00000460551.1:n.565-1G>T
ENST00000621655.1:c.1296G>T	ENSP00000481436.1:n.1296G>T
NM_000243.2:c.1760-1G>T , LRG_190t1:c.1760-1G>T	NP_000234.1:n.1760-1G>T
NM_001198536.1:c.1301G>T	NP_001185465.1:p.Ser434Ile
XM_017023236.2:c.1757-1G>T	XP_016878725.1:n.1757-1G>T
XR_001751903.1:n.2067-1G>T
NM_000243.3:c.1760-1G>T MANE Select	NP_000234.1:n.1760-1G>T
NM_001198536.2:c.1301G>T	NP_001185465.2:p.Ser434Ile