Canonical Allele Identifier: CA2202658501
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3243137G= , CM000678.2:g.3243137G= GRCh38
NC_000016.9:g.3293137G= , CM000678.1:g.3293137G= GRCh37
NC_000016.8:g.3233138G= NCBI36
NG_007871.1:g.18491C= , LRG_190:g.18491C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1471C=
ENST00000219596.6:c.*4C= MANE Select ENSP00000219596.1:n.*4C=
ENST00000219596.5:c.*4C= ENSP00000219596.1:n.*4C=
ENST00000339854.8:c.*4C= ENSP00000339639.4:n.*4C=
ENST00000536980.5:c.*626C= ENSP00000444178.1:n.*626C=
ENST00000537682.5:c.*626C= ENSP00000438611.1:n.*626C=
ENST00000538326.5:c.*975C= ENSP00000437486.1:n.*975C=
ENST00000542898.5:c.*626C= ENSP00000444615.1:n.*626C=
NM_000243.2:c.*4C= , LRG_190t1:c.*4C= NP_000234.1:n.*4C=
NM_001198536.1:c.*554C= NP_001185465.1:n.*554C=
XM_017023236.2:c.*4C= XP_016878725.1:n.*4C=
NM_000243.3:c.*4C= MANE Select NP_000234.1:n.*4C=
NM_001198536.2:c.*554C= NP_001185465.2:n.*554C=