Canonical Allele Identifier: CA2202658610
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243346G= , CM000678.2:g.3243346G= GRCh38
NC_000016.9:g.3293346G= , CM000678.1:g.3293346G= GRCh37
NC_000016.8:g.3233347G= NCBI36
NG_007871.1:g.18282C= , LRG_190:g.18282C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1262C=
ENST00000219596.6:c.2141C= MANE Select ENSP00000219596.1:p.Pro714=
ENST00000219596.5:c.2141C= ENSP00000219596.1:p.Pro714=
ENST00000339854.8:c.1601C= ENSP00000339639.4:p.Pro534=
ENST00000536379.5:c.1508C= ENSP00000445079.1:p.Pro503=
ENST00000536980.5:c.*417C= ENSP00000444178.1:n.*417C=
ENST00000537682.5:c.*417C= ENSP00000438611.1:n.*417C=
ENST00000538326.5:c.*766C= ENSP00000437486.1:n.*766C=
ENST00000539145.5:c.1062C= ENSP00000444471.1:n.1062C=
ENST00000541159.5:c.1683C= ENSP00000438711.1:n.1683C=
ENST00000542898.5:c.*417C= ENSP00000444615.1:n.*417C=
ENST00000570511.5:c.1546C= ENSP00000458312.1:n.1546C=
ENST00000572244.5:c.831C= ENSP00000461186.1:n.831C=
ENST00000574583.5:c.913C= ENSP00000460269.1:n.913C=
ENST00000576315.5:c.946C= ENSP00000460551.1:n.946C=
ENST00000621655.1:c.1678C= ENSP00000481436.1:n.1678C=
NM_000243.2:c.2141C= , LRG_190t1:c.2141C= NP_000234.1:p.Pro714=
NM_001198536.1:c.*345C= NP_001185465.1:n.*345C=
XM_017023236.2:c.2138C= XP_016878725.1:p.Pro713=
NM_000243.3:c.2141C= MANE Select NP_000234.1:p.Pro714=
NM_001198536.2:c.*345C= NP_001185465.2:n.*345C=