Canonical Allele Identifier: CA2202658603
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243335C= , CM000678.2:g.3243335C= GRCh38
NC_000016.9:g.3293335C= , CM000678.1:g.3293335C= GRCh37
NC_000016.8:g.3233336C= NCBI36
NG_007871.1:g.18293G= , LRG_190:g.18293G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1273G=
ENST00000219596.6:c.2152G= MANE Select ENSP00000219596.1:p.Val718=
ENST00000219596.5:c.2152G= ENSP00000219596.1:p.Val718=
ENST00000339854.8:c.1612G= ENSP00000339639.4:p.Val538=
ENST00000536379.5:c.1519G= ENSP00000445079.1:p.Val507=
ENST00000536980.5:c.*428G= ENSP00000444178.1:n.*428G=
ENST00000537682.5:c.*428G= ENSP00000438611.1:n.*428G=
ENST00000538326.5:c.*777G= ENSP00000437486.1:n.*777G=
ENST00000539145.5:c.1073G= ENSP00000444471.1:n.1073G=
ENST00000541159.5:c.1694G= ENSP00000438711.1:n.1694G=
ENST00000542898.5:c.*428G= ENSP00000444615.1:n.*428G=
ENST00000570511.5:c.1557G= ENSP00000458312.1:n.1557G=
ENST00000572244.5:c.842G= ENSP00000461186.1:n.842G=
ENST00000574583.5:c.924G= ENSP00000460269.1:n.924G=
ENST00000576315.5:c.957G= ENSP00000460551.1:n.957G=
ENST00000621655.1:c.1689G= ENSP00000481436.1:n.1689G=
NM_000243.2:c.2152G= , LRG_190t1:c.2152G= NP_000234.1:p.Val718=
NM_001198536.1:c.*356G= NP_001185465.1:n.*356G=
XM_017023236.2:c.2149G= XP_016878725.1:p.Val717=
NM_000243.3:c.2152G= MANE Select NP_000234.1:p.Val718=
NM_001198536.2:c.*356G= NP_001185465.2:n.*356G=