Canonical Allele Identifier: CA493257680

Gene: MEFV

Linked Data

• gnomAD v4: 16-3243174-A-G
• MyVariant Identifiers: chr16:g.3293174A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243174A>G , CM000678.2:g.3243174A>G	GRCh38
NC_000016.9:g.3293174A>G , CM000678.1:g.3293174A>G	GRCh37
NC_000016.8:g.3233175A>G	NCBI36
NG_007871.1:g.18454T>C , LRG_190:g.18454T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1434T>C
ENST00000219596.6:c.2313T>C MANE Select	ENSP00000219596.1:p.Thr771=
ENST00000219596.5:c.2313T>C	ENSP00000219596.1:p.Thr771=
ENST00000339854.8:c.1773T>C	ENSP00000339639.4:p.Thr591=
ENST00000536379.5:c.1680T>C	ENSP00000445079.1:p.Thr560=
ENST00000536980.5:c.*589T>C	ENSP00000444178.1:n.*589T>C
ENST00000537682.5:c.*589T>C	ENSP00000438611.1:n.*589T>C
ENST00000538326.5:c.*938T>C	ENSP00000437486.1:n.*938T>C
ENST00000539145.5:c.1234T>C	ENSP00000444471.1:n.1234T>C
ENST00000541159.5:c.1855T>C	ENSP00000438711.1:n.1855T>C
ENST00000542898.5:c.*589T>C	ENSP00000444615.1:n.*589T>C
ENST00000570511.5:c.1718T>C	ENSP00000458312.1:n.1718T>C
ENST00000572244.5:c.1003T>C	ENSP00000461186.1:n.1003T>C
ENST00000574583.5:c.1085T>C	ENSP00000460269.1:n.1085T>C
ENST00000576315.5:c.1118T>C	ENSP00000460551.1:n.1118T>C
ENST00000621655.1:c.1850T>C	ENSP00000481436.1:n.1850T>C
NM_000243.2:c.2313T>C , LRG_190t1:c.2313T>C	NP_000234.1:p.Thr771=
NM_001198536.1:c.*517T>C	NP_001185465.1:n.*517T>C
XM_017023236.2:c.2310T>C	XP_016878725.1:p.Thr770=
NM_000243.3:c.2313T>C MANE Select	NP_000234.1:p.Thr771=
NM_001198536.2:c.*517T>C	NP_001185465.2:n.*517T>C