Canonical Allele Identifier: CA2202658559
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243254T= , CM000678.2:g.3243254T= GRCh38
NC_000016.9:g.3293254T= , CM000678.1:g.3293254T= GRCh37
NC_000016.8:g.3233255T= NCBI36
NG_007871.1:g.18374A= , LRG_190:g.18374A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1354A=
ENST00000219596.6:c.2233A= MANE Select ENSP00000219596.1:p.Ser745=
ENST00000219596.5:c.2233A= ENSP00000219596.1:p.Ser745=
ENST00000339854.8:c.1693A= ENSP00000339639.4:p.Ser565=
ENST00000536379.5:c.1600A= ENSP00000445079.1:p.Ser534=
ENST00000536980.5:c.*509A= ENSP00000444178.1:n.*509A=
ENST00000537682.5:c.*509A= ENSP00000438611.1:n.*509A=
ENST00000538326.5:c.*858A= ENSP00000437486.1:n.*858A=
ENST00000539145.5:c.1154A= ENSP00000444471.1:n.1154A=
ENST00000541159.5:c.1775A= ENSP00000438711.1:n.1775A=
ENST00000542898.5:c.*509A= ENSP00000444615.1:n.*509A=
ENST00000570511.5:c.1638A= ENSP00000458312.1:n.1638A=
ENST00000572244.5:c.923A= ENSP00000461186.1:n.923A=
ENST00000574583.5:c.1005A= ENSP00000460269.1:n.1005A=
ENST00000576315.5:c.1038A= ENSP00000460551.1:n.1038A=
ENST00000621655.1:c.1770A= ENSP00000481436.1:n.1770A=
NM_000243.2:c.2233A= , LRG_190t1:c.2233A= NP_000234.1:p.Ser745=
NM_001198536.1:c.*437A= NP_001185465.1:n.*437A=
XM_017023236.2:c.2230A= XP_016878725.1:p.Ser744=
NM_000243.3:c.2233A= MANE Select NP_000234.1:p.Ser745=
NM_001198536.2:c.*437A= NP_001185465.2:n.*437A=