Canonical Allele Identifier: CA2573152023

Gene: MEFV

Linked Data

• ClinVar Variation Id: 1607814
• ClinVar RCV Id: RCV002162761
• dbSNP Id: rs1958906845

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244295T>C , CM000678.2:g.3244295T>C	GRCh38
NC_000016.9:g.3294295T>C , CM000678.1:g.3294295T>C	GRCh37
NC_000016.8:g.3234296T>C	NCBI36
NG_007871.1:g.17333A>G , LRG_190:g.17333A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.848-9A>G
ENST00000219596.6:c.1727-9A>G MANE Select	ENSP00000219596.1:n.1727-9A>G
ENST00000219596.5:c.1727-9A>G	ENSP00000219596.1:n.1727-9A>G
ENST00000339854.8:c.1187-9A>G	ENSP00000339639.4:n.1187-9A>G
ENST00000536379.5:c.1094-9A>G	ENSP00000445079.1:n.1094-9A>G
ENST00000536980.5:c.1094-9A>G	ENSP00000444178.1:n.1094-9A>G
ENST00000537682.5:c.1727-9A>G	ENSP00000438611.1:n.1727-9A>G
ENST00000538326.5:c.*352-9A>G	ENSP00000437486.1:n.*352-9A>G
ENST00000539145.5:c.648-9A>G	ENSP00000444471.1:n.648-9A>G
ENST00000541159.5:c.1094-9A>G	ENSP00000438711.1:n.1094-9A>G
ENST00000542898.5:c.1820-9A>G	ENSP00000444615.1:n.1820-9A>G
ENST00000570511.5:c.1165-403A>G	ENSP00000458312.1:n.1165-403A>G
ENST00000572244.5:c.417-9A>G	ENSP00000461186.1:n.417-9A>G
ENST00000574583.5:c.532-403A>G	ENSP00000460269.1:n.532-403A>G
ENST00000576315.5:c.532-9A>G	ENSP00000460551.1:n.532-9A>G
ENST00000621655.1:c.1094-9A>G	ENSP00000481436.1:n.1094-9A>G
NM_000243.2:c.1727-9A>G , LRG_190t1:c.1727-9A>G	NP_000234.1:n.1727-9A>G
NM_001198536.1:c.1094-9A>G	NP_001185465.1:n.1094-9A>G
XM_017023236.2:c.1724-9A>G	XP_016878725.1:n.1724-9A>G
XR_001751903.1:n.1916-9A>G
NM_000243.3:c.1727-9A>G MANE Select	NP_000234.1:n.1727-9A>G
NM_001198536.2:c.1094-9A>G	NP_001185465.2:n.1094-9A>G