Canonical Allele Identifier: CA394485236

Gene: MEFV

Linked Data

• dbSNP Id: rs1567231331
• MyVariant Identifiers: chr16:g.3293280G>T (hg19) ; chr16:g.3243280G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243280G>T , CM000678.2:g.3243280G>T	GRCh38
NC_000016.9:g.3293280G>T , CM000678.1:g.3293280G>T	GRCh37
NC_000016.8:g.3233281G>T	NCBI36
NG_007871.1:g.18348C>A , LRG_190:g.18348C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1328C>A
ENST00000219596.6:c.2207C>A MANE Select	ENSP00000219596.1:p.Ala736Asp
ENST00000219596.5:c.2207C>A	ENSP00000219596.1:p.Ala736Asp
ENST00000339854.8:c.1667C>A	ENSP00000339639.4:p.Ala556Asp
ENST00000536379.5:c.1574C>A	ENSP00000445079.1:p.Ala525Asp
ENST00000536980.5:c.*483C>A	ENSP00000444178.1:n.*483C>A
ENST00000537682.5:c.*483C>A	ENSP00000438611.1:n.*483C>A
ENST00000538326.5:c.*832C>A	ENSP00000437486.1:n.*832C>A
ENST00000539145.5:c.1128C>A	ENSP00000444471.1:n.1128C>A
ENST00000541159.5:c.1749C>A	ENSP00000438711.1:n.1749C>A
ENST00000542898.5:c.*483C>A	ENSP00000444615.1:n.*483C>A
ENST00000570511.5:c.1612C>A	ENSP00000458312.1:n.1612C>A
ENST00000572244.5:c.897C>A	ENSP00000461186.1:n.897C>A
ENST00000574583.5:c.979C>A	ENSP00000460269.1:n.979C>A
ENST00000576315.5:c.1012C>A	ENSP00000460551.1:n.1012C>A
ENST00000621655.1:c.1744C>A	ENSP00000481436.1:n.1744C>A
NM_000243.2:c.2207C>A , LRG_190t1:c.2207C>A	NP_000234.1:p.Ala736Asp
NM_001198536.1:c.*411C>A	NP_001185465.1:n.*411C>A
XM_017023236.2:c.2204C>A	XP_016878725.1:p.Ala735Asp
NM_000243.3:c.2207C>A MANE Select	NP_000234.1:p.Ala736Asp
NM_001198536.2:c.*411C>A	NP_001185465.2:n.*411C>A