Canonical Allele Identifier: CA2202658602
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243333C= , CM000678.2:g.3243333C= GRCh38
NC_000016.9:g.3293333C= , CM000678.1:g.3293333C= GRCh37
NC_000016.8:g.3233334C= NCBI36
NG_007871.1:g.18295G= , LRG_190:g.18295G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697124.1:n.1275G=
ENST00000219596.6:c.2154G= MANE Select ENSP00000219596.1:p.Val718=
ENST00000219596.5:c.2154G= ENSP00000219596.1:p.Val718=
ENST00000339854.8:c.1614G= ENSP00000339639.4:p.Val538=
ENST00000536379.5:c.1521G= ENSP00000445079.1:p.Val507=
ENST00000536980.5:c.*430G= ENSP00000444178.1:n.*430G=
ENST00000537682.5:c.*430G= ENSP00000438611.1:n.*430G=
ENST00000538326.5:c.*779G= ENSP00000437486.1:n.*779G=
ENST00000539145.5:c.1075G= ENSP00000444471.1:n.1075G=
ENST00000541159.5:c.1696G= ENSP00000438711.1:n.1696G=
ENST00000542898.5:c.*430G= ENSP00000444615.1:n.*430G=
ENST00000570511.5:c.1559G= ENSP00000458312.1:n.1559G=
ENST00000572244.5:c.844G= ENSP00000461186.1:n.844G=
ENST00000574583.5:c.926G= ENSP00000460269.1:n.926G=
ENST00000576315.5:c.959G= ENSP00000460551.1:n.959G=
ENST00000621655.1:c.1691G= ENSP00000481436.1:n.1691G=
NM_000243.2:c.2154G= , LRG_190t1:c.2154G= NP_000234.1:p.Val718=
NM_001198536.1:c.*358G= NP_001185465.1:n.*358G=
XM_017023236.2:c.2151G= XP_016878725.1:p.Val717=
NM_000243.3:c.2154G= MANE Select NP_000234.1:p.Val718=
NM_001198536.2:c.*358G= NP_001185465.2:n.*358G=