Canonical Allele Identifier: CA10577521

Gene: MEFV

Linked Data

• ClinVar Variation Id: 234359
• ClinVar RCV Id: RCV000215867 ; RCV002519744
• dbSNP Id: rs876660994
• MyVariant Identifiers: chr16:g.3304491C>T (hg19) ; chr16:g.3254491C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3254491C>T , CM000678.2:g.3254491C>T	GRCh38
NC_000016.9:g.3304491C>T , CM000678.1:g.3304491C>T	GRCh37
NC_000016.8:g.3244492C>T	NCBI36
NG_007871.1:g.7137G>A , LRG_190:g.7137G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.577G>A MANE Select	ENSP00000219596.1:p.Ala193Thr
ENST00000219596.5:c.577G>A	ENSP00000219596.1:p.Ala193Thr
ENST00000339854.8:c.277+1820G>A	ENSP00000339639.4:n.277+1820G>A
ENST00000536379.5:c.277+1820G>A	ENSP00000445079.1:n.277+1820G>A
ENST00000536980.5:c.277+1820G>A	ENSP00000444178.1:n.277+1820G>A
ENST00000537682.5:c.577G>A	ENSP00000438611.1:p.Ala193Thr
ENST00000538326.5:c.577G>A	ENSP00000437486.1:p.Ala193Thr
ENST00000539145.5:c.277+1820G>A	ENSP00000444471.1:n.277+1820G>A
ENST00000541159.5:c.277+1820G>A	ENSP00000438711.1:n.277+1820G>A
ENST00000542898.5:c.577G>A	ENSP00000444615.1:p.Ala193Thr
ENST00000570511.5:c.577G>A	ENSP00000458312.1:p.Ala193Thr
ENST00000572244.5:c.277+1820G>A	ENSP00000461186.1:n.277+1820G>A
ENST00000574583.5:c.277+1820G>A	ENSP00000460269.1:n.277+1820G>A
ENST00000576315.5:c.277+1820G>A	ENSP00000460551.1:n.277+1820G>A
ENST00000621655.1:c.277+1820G>A	ENSP00000481436.1:n.277+1820G>A
NM_000243.2:c.577G>A , LRG_190t1:c.577G>A	NP_000234.1:p.Ala193Thr
NM_001198536.1:c.277+1820G>A	NP_001185465.1:n.277+1820G>A
XM_017023236.2:c.577G>A	XP_016878725.1:p.Ala193Thr
XR_001751903.1:n.766G>A
NM_000243.3:c.577G>A MANE Select	NP_000234.1:p.Ala193Thr
NM_001198536.2:c.277+1820G>A	NP_001185465.2:n.277+1820G>A