Canonical Allele Identifier: CA2631332823

Gene: MEFV

Linked Data

• gnomAD v4: 16-3242887-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242887A>C , CM000678.2:g.3242887A>C	GRCh38
NC_000016.9:g.3292887A>C , CM000678.1:g.3292887A>C	GRCh37
NC_000016.8:g.3232888A>C	NCBI36
NG_007871.1:g.18741T>G , LRG_190:g.18741T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1721T>G
ENST00000219596.6:c.*254T>G MANE Select	ENSP00000219596.1:n.*254T>G
ENST00000219596.5:c.*254T>G	ENSP00000219596.1:n.*254T>G
ENST00000339854.8:c.*254T>G	ENSP00000339639.4:n.*254T>G
ENST00000536980.5:c.*876T>G	ENSP00000444178.1:n.*876T>G
ENST00000537682.5:c.*876T>G	ENSP00000438611.1:n.*876T>G
ENST00000538326.5:c.*1225T>G	ENSP00000437486.1:n.*1225T>G
ENST00000542898.5:c.*876T>G	ENSP00000444615.1:n.*876T>G
NM_000243.2:c.*254T>G , LRG_190t1:c.*254T>G	NP_000234.1:n.*254T>G
NM_001198536.1:c.*804T>G	NP_001185465.1:n.*804T>G
NM_000243.3:c.*254T>G MANE Select	NP_000234.1:n.*254T>G
NM_001198536.2:c.*804T>G	NP_001185465.2:n.*804T>G