Canonical Allele Identifier: CA2805617300
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243042T>A , CM000678.2:g.3243042T>A GRCh38
NC_000016.9:g.3293042T>A , CM000678.1:g.3293042T>A GRCh37
NC_000016.8:g.3233043T>A NCBI36
NG_007871.1:g.18586A>T , LRG_190:g.18586A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1566A>T
ENST00000219596.6:c.*99A>T MANE Select ENSP00000219596.1:n.*99A>T
ENST00000219596.5:c.*99A>T ENSP00000219596.1:n.*99A>T
ENST00000339854.8:c.*99A>T ENSP00000339639.4:n.*99A>T
ENST00000536980.5:c.*721A>T ENSP00000444178.1:n.*721A>T
ENST00000537682.5:c.*721A>T ENSP00000438611.1:n.*721A>T
ENST00000538326.5:c.*1070A>T ENSP00000437486.1:n.*1070A>T
ENST00000542898.5:c.*721A>T ENSP00000444615.1:n.*721A>T
NM_000243.2:c.*99A>T , LRG_190t1:c.*99A>T NP_000234.1:n.*99A>T
NM_001198536.1:c.*649A>T NP_001185465.1:n.*649A>T
NM_000243.3:c.*99A>T MANE Select NP_000234.1:n.*99A>T
NM_001198536.2:c.*649A>T NP_001185465.2:n.*649A>T