Canonical Allele Identifier: CA394481538
Gene: MEFV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3254633G>T , CM000678.2:g.3254633G>T GRCh38
NC_000016.9:g.3304633G>T , CM000678.1:g.3304633G>T GRCh37
NC_000016.8:g.3244634G>T NCBI36
NG_007871.1:g.6995C>A , LRG_190:g.6995C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000219596.6:c.435C>A MANE Select ENSP00000219596.1:p.Ser145Arg
ENST00000219596.5:c.435C>A ENSP00000219596.1:p.Ser145Arg
ENST00000339854.8:c.277+1678C>A ENSP00000339639.4:p.=
ENST00000536379.5:n.277+1678C>A ENSP00000445079.1:p.=
ENST00000536980.5:c.277+1678C>A ENSP00000444178.1:p.=
ENST00000537682.5:c.435C>A ENSP00000438611.1:p.Ser145Arg
ENST00000538326.5:c.435C>A ENSP00000437486.1:p.Ser145Arg
ENST00000539145.5:n.277+1678C>A ENSP00000444471.1:p.=
ENST00000541159.5:n.277+1678C>A ENSP00000438711.1:p.=
ENST00000542898.5:c.435C>A ENSP00000444615.1:p.Ser145Arg
ENST00000570511.5:n.435C>A ENSP00000458312.1:p.Ser145Arg
ENST00000572244.5:n.277+1678C>A ENSP00000461186.1:p.=
ENST00000574583.5:n.277+1678C>A ENSP00000460269.1:p.=
ENST00000576315.5:n.277+1678C>A ENSP00000460551.1:p.=
ENST00000621655.1:n.277+1678C>A ENSP00000481436.1:p.=
NM_000243.2:c.435C>A , LRG_190t1:c.435C>A NP_000234.1:p.Ser145Arg
NM_001198536.1:c.277+1678C>A NP_001185465.1:p.=
XM_017023236.2:c.435C>A XP_016878725.1:p.Ser145Arg
XR_001751903.1:n.624C>A
NM_000243.3:c.435C>A MANE Select NP_000234.1:p.Ser145Arg
NM_001198536.2:c.277+1678C>A NP_001185465.2:p.=