Canonical Allele Identifier: CA2202658715
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243550G= , CM000678.2:g.3243550G= GRCh38
NC_000016.9:g.3293550G= , CM000678.1:g.3293550G= GRCh37
NC_000016.8:g.3233551G= NCBI36
NG_007871.1:g.18078C= , LRG_190:g.18078C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1058C=
ENST00000219596.6:c.1937C= MANE Select ENSP00000219596.1:p.Pro646=
ENST00000219596.5:c.1937C= ENSP00000219596.1:p.Pro646=
ENST00000339854.8:c.1397C= ENSP00000339639.4:p.Pro466=
ENST00000536379.5:c.1304C= ENSP00000445079.1:p.Pro435=
ENST00000536980.5:c.*213C= ENSP00000444178.1:n.*213C=
ENST00000537682.5:c.*213C= ENSP00000438611.1:n.*213C=
ENST00000538326.5:c.*562C= ENSP00000437486.1:n.*562C=
ENST00000539145.5:c.858C= ENSP00000444471.1:n.858C=
ENST00000541159.5:c.1479C= ENSP00000438711.1:n.1479C=
ENST00000542898.5:c.*213C= ENSP00000444615.1:n.*213C=
ENST00000570511.5:c.1342C= ENSP00000458312.1:n.1342C=
ENST00000572244.5:c.627C= ENSP00000461186.1:n.627C=
ENST00000574583.5:c.709C= ENSP00000460269.1:n.709C=
ENST00000576315.5:c.742C= ENSP00000460551.1:n.742C=
ENST00000621655.1:c.1474C= ENSP00000481436.1:n.1474C=
NM_000243.2:c.1937C= , LRG_190t1:c.1937C= NP_000234.1:p.Pro646=
NM_001198536.1:c.*141C= NP_001185465.1:n.*141C=
XM_017023236.2:c.1934C= XP_016878725.1:p.Pro645=
NM_000243.3:c.1937C= MANE Select NP_000234.1:p.Pro646=
NM_001198536.2:c.*141C= NP_001185465.2:n.*141C=