Canonical Allele Identifier: CA394484785

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293218T>A (hg19) ; chr16:g.3243218T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243218T>A , CM000678.2:g.3243218T>A	GRCh38
NC_000016.9:g.3293218T>A , CM000678.1:g.3293218T>A	GRCh37
NC_000016.8:g.3233219T>A	NCBI36
NG_007871.1:g.18410A>T , LRG_190:g.18410A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1390A>T
ENST00000219596.6:c.2269A>T MANE Select	ENSP00000219596.1:p.Ser757Cys
ENST00000219596.5:c.2269A>T	ENSP00000219596.1:p.Ser757Cys
ENST00000339854.8:c.1729A>T	ENSP00000339639.4:p.Ser577Cys
ENST00000536379.5:c.1636A>T	ENSP00000445079.1:p.Ser546Cys
ENST00000536980.5:c.*545A>T	ENSP00000444178.1:n.*545A>T
ENST00000537682.5:c.*545A>T	ENSP00000438611.1:n.*545A>T
ENST00000538326.5:c.*894A>T	ENSP00000437486.1:n.*894A>T
ENST00000539145.5:c.1190A>T	ENSP00000444471.1:n.1190A>T
ENST00000541159.5:c.1811A>T	ENSP00000438711.1:n.1811A>T
ENST00000542898.5:c.*545A>T	ENSP00000444615.1:n.*545A>T
ENST00000570511.5:c.1674A>T	ENSP00000458312.1:n.1674A>T
ENST00000572244.5:c.959A>T	ENSP00000461186.1:n.959A>T
ENST00000574583.5:c.1041A>T	ENSP00000460269.1:n.1041A>T
ENST00000576315.5:c.1074A>T	ENSP00000460551.1:n.1074A>T
ENST00000621655.1:c.1806A>T	ENSP00000481436.1:n.1806A>T
NM_000243.2:c.2269A>T , LRG_190t1:c.2269A>T	NP_000234.1:p.Ser757Cys
NM_001198536.1:c.*473A>T	NP_001185465.1:n.*473A>T
XM_017023236.2:c.2266A>T	XP_016878725.1:p.Ser756Cys
NM_000243.3:c.2269A>T MANE Select	NP_000234.1:p.Ser757Cys
NM_001198536.2:c.*473A>T	NP_001185465.2:n.*473A>T