Canonical Allele Identifier: CA2202658568
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243264A= , CM000678.2:g.3243264A= GRCh38
NC_000016.9:g.3293264A= , CM000678.1:g.3293264A= GRCh37
NC_000016.8:g.3233265A= NCBI36
NG_007871.1:g.18364T= , LRG_190:g.18364T=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1344T=
ENST00000219596.6:c.2223T= MANE Select ENSP00000219596.1:p.Tyr741=
ENST00000219596.5:c.2223T= ENSP00000219596.1:p.Tyr741=
ENST00000339854.8:c.1683T= ENSP00000339639.4:p.Tyr561=
ENST00000536379.5:c.1590T= ENSP00000445079.1:p.Tyr530=
ENST00000536980.5:c.*499T= ENSP00000444178.1:n.*499T=
ENST00000537682.5:c.*499T= ENSP00000438611.1:n.*499T=
ENST00000538326.5:c.*848T= ENSP00000437486.1:n.*848T=
ENST00000539145.5:c.1144T= ENSP00000444471.1:n.1144T=
ENST00000541159.5:c.1765T= ENSP00000438711.1:n.1765T=
ENST00000542898.5:c.*499T= ENSP00000444615.1:n.*499T=
ENST00000570511.5:c.1628T= ENSP00000458312.1:n.1628T=
ENST00000572244.5:c.913T= ENSP00000461186.1:n.913T=
ENST00000574583.5:c.995T= ENSP00000460269.1:n.995T=
ENST00000576315.5:c.1028T= ENSP00000460551.1:n.1028T=
ENST00000621655.1:c.1760T= ENSP00000481436.1:n.1760T=
NM_000243.2:c.2223T= , LRG_190t1:c.2223T= NP_000234.1:p.Tyr741=
NM_001198536.1:c.*427T= NP_001185465.1:n.*427T=
XM_017023236.2:c.2220T= XP_016878725.1:p.Tyr740=
NM_000243.3:c.2223T= MANE Select NP_000234.1:p.Tyr741=
NM_001198536.2:c.*427T= NP_001185465.2:n.*427T=