Canonical Allele Identifier: CA2631332710

Gene: MEFV

Linked Data

• gnomAD v4: 16-3242859-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242859A>C , CM000678.2:g.3242859A>C	GRCh38
NC_000016.9:g.3292859A>C , CM000678.1:g.3292859A>C	GRCh37
NC_000016.8:g.3232860A>C	NCBI36
NG_007871.1:g.18769T>G , LRG_190:g.18769T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1749T>G
ENST00000219596.6:c.*282T>G MANE Select	ENSP00000219596.1:n.*282T>G
ENST00000219596.5:c.*282T>G	ENSP00000219596.1:n.*282T>G
ENST00000339854.8:c.*282T>G	ENSP00000339639.4:n.*282T>G
ENST00000536980.5:c.*904T>G	ENSP00000444178.1:n.*904T>G
ENST00000537682.5:c.*904T>G	ENSP00000438611.1:n.*904T>G
ENST00000538326.5:c.*1253T>G	ENSP00000437486.1:n.*1253T>G
ENST00000542898.5:c.*904T>G	ENSP00000444615.1:n.*904T>G
NM_000243.2:c.*282T>G , LRG_190t1:c.*282T>G	NP_000234.1:n.*282T>G
NM_001198536.1:c.*832T>G	NP_001185465.1:n.*832T>G
NM_000243.3:c.*282T>G MANE Select	NP_000234.1:n.*282T>G
NM_001198536.2:c.*832T>G	NP_001185465.2:n.*832T>G