Canonical Allele Identifier: CA394457829

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3294484T>A (hg19) ; chr16:g.3244484T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244484T>A , CM000678.2:g.3244484T>A	GRCh38
NC_000016.9:g.3294484T>A , CM000678.1:g.3294484T>A	GRCh37
NC_000016.8:g.3234485T>A	NCBI36
NG_007871.1:g.17144A>T , LRG_190:g.17144A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.836A>T
ENST00000219596.6:c.1715A>T MANE Select	ENSP00000219596.1:p.Lys572Met
ENST00000219596.5:c.1715A>T	ENSP00000219596.1:p.Lys572Met
ENST00000339854.8:c.1175A>T	ENSP00000339639.4:p.Lys392Met
ENST00000536379.5:c.1082A>T	ENSP00000445079.1:p.Lys361Met
ENST00000536980.5:c.1082A>T	ENSP00000444178.1:p.Lys361Met
ENST00000537682.5:c.1715A>T	ENSP00000438611.1:p.Lys572Met
ENST00000538326.5:c.*340A>T	ENSP00000437486.1:n.*340A>T
ENST00000539145.5:c.636A>T	ENSP00000444471.1:n.636A>T
ENST00000541159.5:c.1082A>T	ENSP00000438711.1:p.Lys361Met
ENST00000542898.5:c.1808A>T	ENSP00000444615.1:p.Lys603Met
ENST00000570511.5:c.1165-592A>T	ENSP00000458312.1:n.1165-592A>T
ENST00000572244.5:c.405A>T	ENSP00000461186.1:n.405A>T
ENST00000574583.5:c.532-592A>T	ENSP00000460269.1:n.532-592A>T
ENST00000576315.5:c.532-198A>T	ENSP00000460551.1:n.532-198A>T
ENST00000621655.1:c.1082A>T	ENSP00000481436.1:p.Lys361Met
NM_000243.2:c.1715A>T , LRG_190t1:c.1715A>T	NP_000234.1:p.Lys572Met
NM_001198536.1:c.1082A>T	NP_001185465.1:p.Lys361Met
XM_017023236.2:c.1712A>T	XP_016878725.1:p.Lys571Met
XR_001751903.1:n.1904A>T
NM_000243.3:c.1715A>T MANE Select	NP_000234.1:p.Lys572Met
NM_001198536.2:c.1082A>T	NP_001185465.2:p.Lys361Met