Canonical Allele Identifier: CA394485212

Gene: MEFV

Linked Data

• dbSNP Id: rs1958884755
• gnomAD v4: 16-3243274-G-T
• MyVariant Identifiers: chr16:g.3293274G>T (hg19) ; chr16:g.3243274G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243274G>T , CM000678.2:g.3243274G>T	GRCh38
NC_000016.9:g.3293274G>T , CM000678.1:g.3293274G>T	GRCh37
NC_000016.8:g.3233275G>T	NCBI36
NG_007871.1:g.18354C>A , LRG_190:g.18354C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1334C>A
ENST00000219596.6:c.2213C>A MANE Select	ENSP00000219596.1:p.Ser738Tyr
ENST00000219596.5:c.2213C>A	ENSP00000219596.1:p.Ser738Tyr
ENST00000339854.8:c.1673C>A	ENSP00000339639.4:p.Ser558Tyr
ENST00000536379.5:c.1580C>A	ENSP00000445079.1:p.Ser527Tyr
ENST00000536980.5:c.*489C>A	ENSP00000444178.1:n.*489C>A
ENST00000537682.5:c.*489C>A	ENSP00000438611.1:n.*489C>A
ENST00000538326.5:c.*838C>A	ENSP00000437486.1:n.*838C>A
ENST00000539145.5:c.1134C>A	ENSP00000444471.1:n.1134C>A
ENST00000541159.5:c.1755C>A	ENSP00000438711.1:n.1755C>A
ENST00000542898.5:c.*489C>A	ENSP00000444615.1:n.*489C>A
ENST00000570511.5:c.1618C>A	ENSP00000458312.1:n.1618C>A
ENST00000572244.5:c.903C>A	ENSP00000461186.1:n.903C>A
ENST00000574583.5:c.985C>A	ENSP00000460269.1:n.985C>A
ENST00000576315.5:c.1018C>A	ENSP00000460551.1:n.1018C>A
ENST00000621655.1:c.1750C>A	ENSP00000481436.1:n.1750C>A
NM_000243.2:c.2213C>A , LRG_190t1:c.2213C>A	NP_000234.1:p.Ser738Tyr
NM_001198536.1:c.*417C>A	NP_001185465.1:n.*417C>A
XM_017023236.2:c.2210C>A	XP_016878725.1:p.Ser737Tyr
NM_000243.3:c.2213C>A MANE Select	NP_000234.1:p.Ser738Tyr
NM_001198536.2:c.*417C>A	NP_001185465.2:n.*417C>A