Canonical Allele Identifier: CA2202658716
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243552A= , CM000678.2:g.3243552A= GRCh38
NC_000016.9:g.3293552A= , CM000678.1:g.3293552A= GRCh37
NC_000016.8:g.3233553A= NCBI36
NG_007871.1:g.18076T= , LRG_190:g.18076T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1056T=
ENST00000219596.6:c.1935T= MANE Select ENSP00000219596.1:p.Ser645=
ENST00000219596.5:c.1935T= ENSP00000219596.1:p.Ser645=
ENST00000339854.8:c.1395T= ENSP00000339639.4:p.Ser465=
ENST00000536379.5:c.1302T= ENSP00000445079.1:p.Ser434=
ENST00000536980.5:c.*211T= ENSP00000444178.1:n.*211T=
ENST00000537682.5:c.*211T= ENSP00000438611.1:n.*211T=
ENST00000538326.5:c.*560T= ENSP00000437486.1:n.*560T=
ENST00000539145.5:c.856T= ENSP00000444471.1:n.856T=
ENST00000541159.5:c.1477T= ENSP00000438711.1:n.1477T=
ENST00000542898.5:c.*211T= ENSP00000444615.1:n.*211T=
ENST00000570511.5:c.1340T= ENSP00000458312.1:n.1340T=
ENST00000572244.5:c.625T= ENSP00000461186.1:n.625T=
ENST00000574583.5:c.707T= ENSP00000460269.1:n.707T=
ENST00000576315.5:c.740T= ENSP00000460551.1:n.740T=
ENST00000621655.1:c.1472T= ENSP00000481436.1:n.1472T=
NM_000243.2:c.1935T= , LRG_190t1:c.1935T= NP_000234.1:p.Ser645=
NM_001198536.1:c.*139T= NP_001185465.1:n.*139T=
XM_017023236.2:c.1932T= XP_016878725.1:p.Ser644=
NM_000243.3:c.1935T= MANE Select NP_000234.1:p.Ser645=
NM_001198536.2:c.*139T= NP_001185465.2:n.*139T=