Canonical Allele Identifier: CA394464204
Gene: MEFV HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3297144C>A (hg19) chr16:g.3247144C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3247144C>A , CM000678.2:g.3247144C>A GRCh38
NC_000016.9:g.3297144C>A , CM000678.1:g.3297144C>A GRCh37
NC_000016.8:g.3237145C>A NCBI36
NG_007871.1:g.14484G>T , LRG_190:g.14484G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000219596.6:c.1459G>T MANE Select ENSP00000219596.1:p.Val487Leu
ENST00000219596.5:c.1459G>T ENSP00000219596.1:p.Val487Leu
ENST00000339854.8:c.919G>T ENSP00000339639.4:p.Val307Leu
ENST00000536379.5:c.826G>T ENSP00000445079.1:p.Val276Leu
ENST00000536980.5:c.826G>T ENSP00000444178.1:p.Val276Leu
ENST00000537682.5:c.1459G>T ENSP00000438611.1:p.Val487Leu
ENST00000538326.5:c.*84G>T ENSP00000437486.1:n.*84G>T
ENST00000539145.5:c.380G>T ENSP00000444471.1:n.380G>T
ENST00000539154.1:n.824G>T
ENST00000541159.5:c.826G>T ENSP00000438711.1:p.Val276Leu
ENST00000542898.5:c.1552G>T ENSP00000444615.1:p.Val518Leu
ENST00000570511.5:c.1013G>T ENSP00000458312.1:n.1013G>T
ENST00000572244.5:c.278-597G>T ENSP00000461186.1:n.278-597G>T
ENST00000574583.5:c.380G>T ENSP00000460269.1:n.380G>T
ENST00000576315.5:c.380G>T ENSP00000460551.1:n.380G>T
ENST00000621655.1:c.826G>T ENSP00000481436.1:p.Val276Leu
NM_000243.2:c.1459G>T , LRG_190t1:c.1459G>T NP_000234.1:p.Val487Leu
NM_001198536.1:c.826G>T NP_001185465.1:p.Val276Leu
XM_017023236.2:c.1456G>T XP_016878725.1:p.Val486Leu
XR_001751903.1:n.1648G>T
NM_000243.3:c.1459G>T MANE Select NP_000234.1:p.Val487Leu
NM_001198536.2:c.826G>T NP_001185465.2:p.Val276Leu
Search 100 bp 5'
Search 100 bp 3'