Canonical Allele Identifier: CA394484763

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293215G>T (hg19) ; chr16:g.3243215G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243215G>T , CM000678.2:g.3243215G>T	GRCh38
NC_000016.9:g.3293215G>T , CM000678.1:g.3293215G>T	GRCh37
NC_000016.8:g.3233216G>T	NCBI36
NG_007871.1:g.18413C>A , LRG_190:g.18413C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1393C>A
ENST00000219596.6:c.2272C>A MANE Select	ENSP00000219596.1:p.Pro758Thr
ENST00000219596.5:c.2272C>A	ENSP00000219596.1:p.Pro758Thr
ENST00000339854.8:c.1732C>A	ENSP00000339639.4:p.Pro578Thr
ENST00000536379.5:c.1639C>A	ENSP00000445079.1:p.Pro547Thr
ENST00000536980.5:c.*548C>A	ENSP00000444178.1:n.*548C>A
ENST00000537682.5:c.*548C>A	ENSP00000438611.1:n.*548C>A
ENST00000538326.5:c.*897C>A	ENSP00000437486.1:n.*897C>A
ENST00000539145.5:c.1193C>A	ENSP00000444471.1:n.1193C>A
ENST00000541159.5:c.1814C>A	ENSP00000438711.1:n.1814C>A
ENST00000542898.5:c.*548C>A	ENSP00000444615.1:n.*548C>A
ENST00000570511.5:c.1677C>A	ENSP00000458312.1:n.1677C>A
ENST00000572244.5:c.962C>A	ENSP00000461186.1:n.962C>A
ENST00000574583.5:c.1044C>A	ENSP00000460269.1:n.1044C>A
ENST00000576315.5:c.1077C>A	ENSP00000460551.1:n.1077C>A
ENST00000621655.1:c.1809C>A	ENSP00000481436.1:n.1809C>A
NM_000243.2:c.2272C>A , LRG_190t1:c.2272C>A	NP_000234.1:p.Pro758Thr
NM_001198536.1:c.*476C>A	NP_001185465.1:n.*476C>A
XM_017023236.2:c.2269C>A	XP_016878725.1:p.Pro757Thr
NM_000243.3:c.2272C>A MANE Select	NP_000234.1:p.Pro758Thr
NM_001198536.2:c.*476C>A	NP_001185465.2:n.*476C>A