Canonical Allele Identifier: CA2202658367
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3242881G= , CM000678.2:g.3242881G= GRCh38
NC_000016.9:g.3292881G= , CM000678.1:g.3292881G= GRCh37
NC_000016.8:g.3232882G= NCBI36
NG_007871.1:g.18747C= , LRG_190:g.18747C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1727C=
ENST00000219596.6:c.*260C= MANE Select ENSP00000219596.1:n.*260C=
ENST00000219596.5:c.*260C= ENSP00000219596.1:n.*260C=
ENST00000339854.8:c.*260C= ENSP00000339639.4:n.*260C=
ENST00000536980.5:c.*882C= ENSP00000444178.1:n.*882C=
ENST00000537682.5:c.*882C= ENSP00000438611.1:n.*882C=
ENST00000538326.5:c.*1231C= ENSP00000437486.1:n.*1231C=
ENST00000542898.5:c.*882C= ENSP00000444615.1:n.*882C=
NM_000243.2:c.*260C= , LRG_190t1:c.*260C= NP_000234.1:n.*260C=
NM_001198536.1:c.*810C= NP_001185465.1:n.*810C=
NM_000243.3:c.*260C= MANE Select NP_000234.1:n.*260C=
NM_001198536.2:c.*810C= NP_001185465.2:n.*810C=