Canonical Allele Identifier: CA2631332735

Gene: MEFV

Linked Data

• gnomAD v4: 16-3242864-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242864A>G , CM000678.2:g.3242864A>G	GRCh38
NC_000016.9:g.3292864A>G , CM000678.1:g.3292864A>G	GRCh37
NC_000016.8:g.3232865A>G	NCBI36
NG_007871.1:g.18764T>C , LRG_190:g.18764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1744T>C
ENST00000219596.6:c.*277T>C MANE Select	ENSP00000219596.1:n.*277T>C
ENST00000219596.5:c.*277T>C	ENSP00000219596.1:n.*277T>C
ENST00000339854.8:c.*277T>C	ENSP00000339639.4:n.*277T>C
ENST00000536980.5:c.*899T>C	ENSP00000444178.1:n.*899T>C
ENST00000537682.5:c.*899T>C	ENSP00000438611.1:n.*899T>C
ENST00000538326.5:c.*1248T>C	ENSP00000437486.1:n.*1248T>C
ENST00000542898.5:c.*899T>C	ENSP00000444615.1:n.*899T>C
NM_000243.2:c.*277T>C , LRG_190t1:c.*277T>C	NP_000234.1:n.*277T>C
NM_001198536.1:c.*827T>C	NP_001185465.1:n.*827T>C
NM_000243.3:c.*277T>C MANE Select	NP_000234.1:n.*277T>C
NM_001198536.2:c.*827T>C	NP_001185465.2:n.*827T>C