Canonical Allele Identifier: CA2550683007
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243015A>T , CM000678.2:g.3243015A>T GRCh38
NC_000016.9:g.3293015A>T , CM000678.1:g.3293015A>T GRCh37
NC_000016.8:g.3233016A>T NCBI36
NG_007871.1:g.18613T>A , LRG_190:g.18613T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1593T>A
ENST00000219596.6:c.*126T>A MANE Select ENSP00000219596.1:n.*126T>A
ENST00000219596.5:c.*126T>A ENSP00000219596.1:n.*126T>A
ENST00000339854.8:c.*126T>A ENSP00000339639.4:n.*126T>A
ENST00000536980.5:c.*748T>A ENSP00000444178.1:n.*748T>A
ENST00000537682.5:c.*748T>A ENSP00000438611.1:n.*748T>A
ENST00000538326.5:c.*1097T>A ENSP00000437486.1:n.*1097T>A
ENST00000542898.5:c.*748T>A ENSP00000444615.1:n.*748T>A
NM_000243.2:c.*126T>A , LRG_190t1:c.*126T>A NP_000234.1:n.*126T>A
NM_001198536.1:c.*676T>A NP_001185465.1:n.*676T>A
NM_000243.3:c.*126T>A MANE Select NP_000234.1:n.*126T>A
NM_001198536.2:c.*676T>A NP_001185465.2:n.*676T>A