Canonical Allele Identifier: CA2631332748

Gene: MEFV

Linked Data

• gnomAD v4: 16-3242868-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242868T>G , CM000678.2:g.3242868T>G	GRCh38
NC_000016.9:g.3292868T>G , CM000678.1:g.3292868T>G	GRCh37
NC_000016.8:g.3232869T>G	NCBI36
NG_007871.1:g.18760A>C , LRG_190:g.18760A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1740A>C
ENST00000219596.6:c.*273A>C MANE Select	ENSP00000219596.1:n.*273A>C
ENST00000219596.5:c.*273A>C	ENSP00000219596.1:n.*273A>C
ENST00000339854.8:c.*273A>C	ENSP00000339639.4:n.*273A>C
ENST00000536980.5:c.*895A>C	ENSP00000444178.1:n.*895A>C
ENST00000537682.5:c.*895A>C	ENSP00000438611.1:n.*895A>C
ENST00000538326.5:c.*1244A>C	ENSP00000437486.1:n.*1244A>C
ENST00000542898.5:c.*895A>C	ENSP00000444615.1:n.*895A>C
NM_000243.2:c.*273A>C , LRG_190t1:c.*273A>C	NP_000234.1:n.*273A>C
NM_001198536.1:c.*823A>C	NP_001185465.1:n.*823A>C
NM_000243.3:c.*273A>C MANE Select	NP_000234.1:n.*273A>C
NM_001198536.2:c.*823A>C	NP_001185465.2:n.*823A>C