Canonical Allele Identifier: CA493257474

Gene: MEFV

Linked Data

• gnomAD v4: 16-3243153-C-T
• MyVariant Identifiers: chr16:g.3293153C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243153C>T , CM000678.2:g.3243153C>T	GRCh38
NC_000016.9:g.3293153C>T , CM000678.1:g.3293153C>T	GRCh37
NC_000016.8:g.3233154C>T	NCBI36
NG_007871.1:g.18475G>A , LRG_190:g.18475G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1455G>A
ENST00000219596.6:c.2334G>A MANE Select	ENSP00000219596.1:p.Gln778=
ENST00000219596.5:c.2334G>A	ENSP00000219596.1:p.Gln778=
ENST00000339854.8:c.1794G>A	ENSP00000339639.4:p.Gln598=
ENST00000536379.5:c.1701G>A	ENSP00000445079.1:p.Gln567=
ENST00000536980.5:c.*610G>A	ENSP00000444178.1:n.*610G>A
ENST00000537682.5:c.*610G>A	ENSP00000438611.1:n.*610G>A
ENST00000538326.5:c.*959G>A	ENSP00000437486.1:n.*959G>A
ENST00000539145.5:c.1255G>A	ENSP00000444471.1:n.1255G>A
ENST00000541159.5:c.1876G>A	ENSP00000438711.1:n.1876G>A
ENST00000542898.5:c.*610G>A	ENSP00000444615.1:n.*610G>A
ENST00000570511.5:c.1739G>A	ENSP00000458312.1:n.1739G>A
ENST00000572244.5:c.1024G>A	ENSP00000461186.1:n.1024G>A
ENST00000574583.5:c.1106G>A	ENSP00000460269.1:n.1106G>A
ENST00000576315.5:c.1139G>A	ENSP00000460551.1:n.1139G>A
ENST00000621655.1:c.1871G>A	ENSP00000481436.1:n.1871G>A
NM_000243.2:c.2334G>A , LRG_190t1:c.2334G>A	NP_000234.1:p.Gln778=
NM_001198536.1:c.*538G>A	NP_001185465.1:n.*538G>A
XM_017023236.2:c.2331G>A	XP_016878725.1:p.Gln777=
NM_000243.3:c.2334G>A MANE Select	NP_000234.1:p.Gln778=
NM_001198536.2:c.*538G>A	NP_001185465.2:n.*538G>A