Canonical Allele Identifier: CA394485677

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293334A>C (hg19) ; chr16:g.3243334A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243334A>C , CM000678.2:g.3243334A>C	GRCh38
NC_000016.9:g.3293334A>C , CM000678.1:g.3293334A>C	GRCh37
NC_000016.8:g.3233335A>C	NCBI36
NG_007871.1:g.18294T>G , LRG_190:g.18294T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1274T>G
ENST00000219596.6:c.2153T>G MANE Select	ENSP00000219596.1:p.Val718Gly
ENST00000219596.5:c.2153T>G	ENSP00000219596.1:p.Val718Gly
ENST00000339854.8:c.1613T>G	ENSP00000339639.4:p.Val538Gly
ENST00000536379.5:c.1520T>G	ENSP00000445079.1:p.Val507Gly
ENST00000536980.5:c.*429T>G	ENSP00000444178.1:n.*429T>G
ENST00000537682.5:c.*429T>G	ENSP00000438611.1:n.*429T>G
ENST00000538326.5:c.*778T>G	ENSP00000437486.1:n.*778T>G
ENST00000539145.5:c.1074T>G	ENSP00000444471.1:n.1074T>G
ENST00000541159.5:c.1695T>G	ENSP00000438711.1:n.1695T>G
ENST00000542898.5:c.*429T>G	ENSP00000444615.1:n.*429T>G
ENST00000570511.5:c.1558T>G	ENSP00000458312.1:n.1558T>G
ENST00000572244.5:c.843T>G	ENSP00000461186.1:n.843T>G
ENST00000574583.5:c.925T>G	ENSP00000460269.1:n.925T>G
ENST00000576315.5:c.958T>G	ENSP00000460551.1:n.958T>G
ENST00000621655.1:c.1690T>G	ENSP00000481436.1:n.1690T>G
NM_000243.2:c.2153T>G , LRG_190t1:c.2153T>G	NP_000234.1:p.Val718Gly
NM_001198536.1:c.*357T>G	NP_001185465.1:n.*357T>G
XM_017023236.2:c.2150T>G	XP_016878725.1:p.Val717Gly
NM_000243.3:c.2153T>G MANE Select	NP_000234.1:p.Val718Gly
NM_001198536.2:c.*357T>G	NP_001185465.2:n.*357T>G