Canonical Allele Identifier: CA394463569

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3297081G>T (hg19) ; chr16:g.3247081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247081G>T , CM000678.2:g.3247081G>T	GRCh38
NC_000016.9:g.3297081G>T , CM000678.1:g.3297081G>T	GRCh37
NC_000016.8:g.3237082G>T	NCBI36
NG_007871.1:g.14547C>A , LRG_190:g.14547C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000219596.6:c.1522C>A MANE Select	ENSP00000219596.1:p.Leu508Met
ENST00000219596.5:c.1522C>A	ENSP00000219596.1:p.Leu508Met
ENST00000339854.8:c.982C>A	ENSP00000339639.4:p.Leu328Met
ENST00000536379.5:c.889C>A	ENSP00000445079.1:p.Leu297Met
ENST00000536980.5:c.889C>A	ENSP00000444178.1:p.Leu297Met
ENST00000537682.5:c.1522C>A	ENSP00000438611.1:p.Leu508Met
ENST00000538326.5:c.*147C>A	ENSP00000437486.1:n.*147C>A
ENST00000539145.5:c.443C>A	ENSP00000444471.1:n.443C>A
ENST00000539154.1:n.887C>A
ENST00000541159.5:c.889C>A	ENSP00000438711.1:p.Leu297Met
ENST00000542898.5:c.1615C>A	ENSP00000444615.1:p.Leu539Met
ENST00000570511.5:c.1076C>A	ENSP00000458312.1:n.1076C>A
ENST00000572244.5:c.278-534C>A	ENSP00000461186.1:n.278-534C>A
ENST00000574583.5:c.443C>A	ENSP00000460269.1:n.443C>A
ENST00000576315.5:c.443C>A	ENSP00000460551.1:n.443C>A
ENST00000621655.1:c.889C>A	ENSP00000481436.1:p.Leu297Met
NM_000243.2:c.1522C>A , LRG_190t1:c.1522C>A	NP_000234.1:p.Leu508Met
NM_001198536.1:c.889C>A	NP_001185465.1:p.Leu297Met
XM_017023236.2:c.1519C>A	XP_016878725.1:p.Leu507Met
XR_001751903.1:n.1711C>A
NM_000243.3:c.1522C>A MANE Select	NP_000234.1:p.Leu508Met
NM_001198536.2:c.889C>A	NP_001185465.2:p.Leu297Met