Canonical Allele Identifier: CA2202658589
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243304C= , CM000678.2:g.3243304C= GRCh38
NC_000016.9:g.3293304C= , CM000678.1:g.3293304C= GRCh37
NC_000016.8:g.3233305C= NCBI36
NG_007871.1:g.18324G= , LRG_190:g.18324G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1304G=
ENST00000219596.6:c.2183G= MANE Select ENSP00000219596.1:p.Ser728=
ENST00000219596.5:c.2183G= ENSP00000219596.1:p.Ser728=
ENST00000339854.8:c.1643G= ENSP00000339639.4:p.Ser548=
ENST00000536379.5:c.1550G= ENSP00000445079.1:p.Ser517=
ENST00000536980.5:c.*459G= ENSP00000444178.1:n.*459G=
ENST00000537682.5:c.*459G= ENSP00000438611.1:n.*459G=
ENST00000538326.5:c.*808G= ENSP00000437486.1:n.*808G=
ENST00000539145.5:c.1104G= ENSP00000444471.1:n.1104G=
ENST00000541159.5:c.1725G= ENSP00000438711.1:n.1725G=
ENST00000542898.5:c.*459G= ENSP00000444615.1:n.*459G=
ENST00000570511.5:c.1588G= ENSP00000458312.1:n.1588G=
ENST00000572244.5:c.873G= ENSP00000461186.1:n.873G=
ENST00000574583.5:c.955G= ENSP00000460269.1:n.955G=
ENST00000576315.5:c.988G= ENSP00000460551.1:n.988G=
ENST00000621655.1:c.1720G= ENSP00000481436.1:n.1720G=
NM_000243.2:c.2183G= , LRG_190t1:c.2183G= NP_000234.1:p.Ser728=
NM_001198536.1:c.*387G= NP_001185465.1:n.*387G=
XM_017023236.2:c.2180G= XP_016878725.1:p.Ser727=
NM_000243.3:c.2183G= MANE Select NP_000234.1:p.Ser728=
NM_001198536.2:c.*387G= NP_001185465.2:n.*387G=