Canonical Allele Identifier: CA394484861

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293226G>T (hg19) ; chr16:g.3243226G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243226G>T , CM000678.2:g.3243226G>T	GRCh38
NC_000016.9:g.3293226G>T , CM000678.1:g.3293226G>T	GRCh37
NC_000016.8:g.3233227G>T	NCBI36
NG_007871.1:g.18402C>A , LRG_190:g.18402C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1382C>A
ENST00000219596.6:c.2261C>A MANE Select	ENSP00000219596.1:p.Pro754His
ENST00000219596.5:c.2261C>A	ENSP00000219596.1:p.Pro754His
ENST00000339854.8:c.1721C>A	ENSP00000339639.4:p.Pro574His
ENST00000536379.5:c.1628C>A	ENSP00000445079.1:p.Pro543His
ENST00000536980.5:c.*537C>A	ENSP00000444178.1:n.*537C>A
ENST00000537682.5:c.*537C>A	ENSP00000438611.1:n.*537C>A
ENST00000538326.5:c.*886C>A	ENSP00000437486.1:n.*886C>A
ENST00000539145.5:c.1182C>A	ENSP00000444471.1:n.1182C>A
ENST00000541159.5:c.1803C>A	ENSP00000438711.1:n.1803C>A
ENST00000542898.5:c.*537C>A	ENSP00000444615.1:n.*537C>A
ENST00000570511.5:c.1666C>A	ENSP00000458312.1:n.1666C>A
ENST00000572244.5:c.951C>A	ENSP00000461186.1:n.951C>A
ENST00000574583.5:c.1033C>A	ENSP00000460269.1:n.1033C>A
ENST00000576315.5:c.1066C>A	ENSP00000460551.1:n.1066C>A
ENST00000621655.1:c.1798C>A	ENSP00000481436.1:n.1798C>A
NM_000243.2:c.2261C>A , LRG_190t1:c.2261C>A	NP_000234.1:p.Pro754His
NM_001198536.1:c.*465C>A	NP_001185465.1:n.*465C>A
XM_017023236.2:c.2258C>A	XP_016878725.1:p.Pro753His
NM_000243.3:c.2261C>A MANE Select	NP_000234.1:p.Pro754His
NM_001198536.2:c.*465C>A	NP_001185465.2:n.*465C>A