Canonical Allele Identifier: CA2202658409
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3242966A= , CM000678.2:g.3242966A= GRCh38
NC_000016.9:g.3292966A= , CM000678.1:g.3292966A= GRCh37
NC_000016.8:g.3232967A= NCBI36
NG_007871.1:g.18662T= , LRG_190:g.18662T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697124.1:n.1642T=
ENST00000219596.6:c.*175T= MANE Select ENSP00000219596.1:n.*175T=
ENST00000219596.5:c.*175T= ENSP00000219596.1:n.*175T=
ENST00000339854.8:c.*175T= ENSP00000339639.4:n.*175T=
ENST00000536980.5:c.*797T= ENSP00000444178.1:n.*797T=
ENST00000537682.5:c.*797T= ENSP00000438611.1:n.*797T=
ENST00000538326.5:c.*1146T= ENSP00000437486.1:n.*1146T=
ENST00000542898.5:c.*797T= ENSP00000444615.1:n.*797T=
NM_000243.2:c.*175T= , LRG_190t1:c.*175T= NP_000234.1:n.*175T=
NM_001198536.1:c.*725T= NP_001185465.1:n.*725T=
NM_000243.3:c.*175T= MANE Select NP_000234.1:n.*175T=
NM_001198536.2:c.*725T= NP_001185465.2:n.*725T=