Canonical Allele Identifier: CA394485582

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293319T>A (hg19) ; chr16:g.3243319T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243319T>A , CM000678.2:g.3243319T>A	GRCh38
NC_000016.9:g.3293319T>A , CM000678.1:g.3293319T>A	GRCh37
NC_000016.8:g.3233320T>A	NCBI36
NG_007871.1:g.18309A>T , LRG_190:g.18309A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1289A>T
ENST00000219596.6:c.2168A>T MANE Select	ENSP00000219596.1:p.Asp723Val
ENST00000219596.5:c.2168A>T	ENSP00000219596.1:p.Asp723Val
ENST00000339854.8:c.1628A>T	ENSP00000339639.4:p.Asp543Val
ENST00000536379.5:c.1535A>T	ENSP00000445079.1:p.Asp512Val
ENST00000536980.5:c.*444A>T	ENSP00000444178.1:n.*444A>T
ENST00000537682.5:c.*444A>T	ENSP00000438611.1:n.*444A>T
ENST00000538326.5:c.*793A>T	ENSP00000437486.1:n.*793A>T
ENST00000539145.5:c.1089A>T	ENSP00000444471.1:n.1089A>T
ENST00000541159.5:c.1710A>T	ENSP00000438711.1:n.1710A>T
ENST00000542898.5:c.*444A>T	ENSP00000444615.1:n.*444A>T
ENST00000570511.5:c.1573A>T	ENSP00000458312.1:n.1573A>T
ENST00000572244.5:c.858A>T	ENSP00000461186.1:n.858A>T
ENST00000574583.5:c.940A>T	ENSP00000460269.1:n.940A>T
ENST00000576315.5:c.973A>T	ENSP00000460551.1:n.973A>T
ENST00000621655.1:c.1705A>T	ENSP00000481436.1:n.1705A>T
NM_000243.2:c.2168A>T , LRG_190t1:c.2168A>T	NP_000234.1:p.Asp723Val
NM_001198536.1:c.*372A>T	NP_001185465.1:n.*372A>T
XM_017023236.2:c.2165A>T	XP_016878725.1:p.Asp722Val
NM_000243.3:c.2168A>T MANE Select	NP_000234.1:p.Asp723Val
NM_001198536.2:c.*372A>T	NP_001185465.2:n.*372A>T