Canonical Allele Identifier: CA493258129

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293255G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243255G>A , CM000678.2:g.3243255G>A	GRCh38
NC_000016.9:g.3293255G>A , CM000678.1:g.3293255G>A	GRCh37
NC_000016.8:g.3233256G>A	NCBI36
NG_007871.1:g.18373C>T , LRG_190:g.18373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1353C>T
ENST00000219596.6:c.2232C>T MANE Select	ENSP00000219596.1:p.Ala744=
ENST00000219596.5:c.2232C>T	ENSP00000219596.1:p.Ala744=
ENST00000339854.8:c.1692C>T	ENSP00000339639.4:p.Ala564=
ENST00000536379.5:c.1599C>T	ENSP00000445079.1:p.Ala533=
ENST00000536980.5:c.*508C>T	ENSP00000444178.1:n.*508C>T
ENST00000537682.5:c.*508C>T	ENSP00000438611.1:n.*508C>T
ENST00000538326.5:c.*857C>T	ENSP00000437486.1:n.*857C>T
ENST00000539145.5:c.1153C>T	ENSP00000444471.1:n.1153C>T
ENST00000541159.5:c.1774C>T	ENSP00000438711.1:n.1774C>T
ENST00000542898.5:c.*508C>T	ENSP00000444615.1:n.*508C>T
ENST00000570511.5:c.1637C>T	ENSP00000458312.1:n.1637C>T
ENST00000572244.5:c.922C>T	ENSP00000461186.1:n.922C>T
ENST00000574583.5:c.1004C>T	ENSP00000460269.1:n.1004C>T
ENST00000576315.5:c.1037C>T	ENSP00000460551.1:n.1037C>T
ENST00000621655.1:c.1769C>T	ENSP00000481436.1:n.1769C>T
NM_000243.2:c.2232C>T , LRG_190t1:c.2232C>T	NP_000234.1:p.Ala744=
NM_001198536.1:c.*436C>T	NP_001185465.1:n.*436C>T
XM_017023236.2:c.2229C>T	XP_016878725.1:p.Ala743=
NM_000243.3:c.2232C>T MANE Select	NP_000234.1:p.Ala744=
NM_001198536.2:c.*436C>T	NP_001185465.2:n.*436C>T