Canonical Allele Identifier: CA394487823

Gene: MEFV

Linked Data

• dbSNP Id: rs369107119
• gnomAD v4: 16-3243585-T-G
• MyVariant Identifiers: chr16:g.3293585T>G (hg19) ; chr16:g.3243585T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243585T>G , CM000678.2:g.3243585T>G	GRCh38
NC_000016.9:g.3293585T>G , CM000678.1:g.3293585T>G	GRCh37
NC_000016.8:g.3233586T>G	NCBI36
NG_007871.1:g.18043A>C , LRG_190:g.18043A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1023A>C
ENST00000219596.6:c.1902A>C MANE Select	ENSP00000219596.1:p.Gln634His
ENST00000219596.5:c.1902A>C	ENSP00000219596.1:p.Gln634His
ENST00000339854.8:c.1362A>C	ENSP00000339639.4:p.Gln454His
ENST00000536379.5:c.1269A>C	ENSP00000445079.1:p.Gln423His
ENST00000536980.5:c.*178A>C	ENSP00000444178.1:n.*178A>C
ENST00000537682.5:c.*178A>C	ENSP00000438611.1:n.*178A>C
ENST00000538326.5:c.*527A>C	ENSP00000437486.1:n.*527A>C
ENST00000539145.5:c.823A>C	ENSP00000444471.1:n.823A>C
ENST00000541159.5:c.1444A>C	ENSP00000438711.1:n.1444A>C
ENST00000542898.5:c.*178A>C	ENSP00000444615.1:n.*178A>C
ENST00000570511.5:c.1307A>C	ENSP00000458312.1:n.1307A>C
ENST00000572244.5:c.592A>C	ENSP00000461186.1:n.592A>C
ENST00000574583.5:c.674A>C	ENSP00000460269.1:n.674A>C
ENST00000576315.5:c.707A>C	ENSP00000460551.1:n.707A>C
ENST00000621655.1:c.1439A>C	ENSP00000481436.1:n.1439A>C
NM_000243.2:c.1902A>C , LRG_190t1:c.1902A>C	NP_000234.1:p.Gln634His
NM_001198536.1:c.*106A>C	NP_001185465.1:n.*106A>C
XM_017023236.2:c.1899A>C	XP_016878725.1:p.Gln633His
NM_000243.3:c.1902A>C MANE Select	NP_000234.1:p.Gln634His
NM_001198536.2:c.*106A>C	NP_001185465.2:n.*106A>C