Canonical Allele Identifier: CA2202658583
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243293A= , CM000678.2:g.3243293A= GRCh38
NC_000016.9:g.3293293A= , CM000678.1:g.3293293A= GRCh37
NC_000016.8:g.3233294A= NCBI36
NG_007871.1:g.18335T= , LRG_190:g.18335T=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1315T=
ENST00000219596.6:c.2194T= MANE Select ENSP00000219596.1:p.Tyr732=
ENST00000219596.5:c.2194T= ENSP00000219596.1:p.Tyr732=
ENST00000339854.8:c.1654T= ENSP00000339639.4:p.Tyr552=
ENST00000536379.5:c.1561T= ENSP00000445079.1:p.Tyr521=
ENST00000536980.5:c.*470T= ENSP00000444178.1:n.*470T=
ENST00000537682.5:c.*470T= ENSP00000438611.1:n.*470T=
ENST00000538326.5:c.*819T= ENSP00000437486.1:n.*819T=
ENST00000539145.5:c.1115T= ENSP00000444471.1:n.1115T=
ENST00000541159.5:c.1736T= ENSP00000438711.1:n.1736T=
ENST00000542898.5:c.*470T= ENSP00000444615.1:n.*470T=
ENST00000570511.5:c.1599T= ENSP00000458312.1:n.1599T=
ENST00000572244.5:c.884T= ENSP00000461186.1:n.884T=
ENST00000574583.5:c.966T= ENSP00000460269.1:n.966T=
ENST00000576315.5:c.999T= ENSP00000460551.1:n.999T=
ENST00000621655.1:c.1731T= ENSP00000481436.1:n.1731T=
NM_000243.2:c.2194T= , LRG_190t1:c.2194T= NP_000234.1:p.Tyr732=
NM_001198536.1:c.*398T= NP_001185465.1:n.*398T=
XM_017023236.2:c.2191T= XP_016878725.1:p.Tyr731=
NM_000243.3:c.2194T= MANE Select NP_000234.1:p.Tyr732=
NM_001198536.2:c.*398T= NP_001185465.2:n.*398T=