Canonical Allele Identifier: CA280409

Gene: MEFV

Linked Data

• ClinVar Variation Id: 97447
• ClinVar RCV Id: RCV000083699 ; RCV002483160 ; RCV003126429 ; RCV003126430
• dbSNP Id: rs104895101
• MyVariant Identifiers: chr16:g.3297102G>C (hg19) ; chr16:g.3247102G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3247102G>C , CM000678.2:g.3247102G>C	GRCh38
NC_000016.9:g.3297102G>C , CM000678.1:g.3297102G>C	GRCh37
NC_000016.8:g.3237103G>C	NCBI36
NG_007871.1:g.14526C>G , LRG_190:g.14526C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.1501C>G MANE Select	ENSP00000219596.1:p.Arg501Gly
ENST00000219596.5:c.1501C>G	ENSP00000219596.1:p.Arg501Gly
ENST00000339854.8:c.961C>G	ENSP00000339639.4:p.Arg321Gly
ENST00000536379.5:c.868C>G	ENSP00000445079.1:p.Arg290Gly
ENST00000536980.5:c.868C>G	ENSP00000444178.1:p.Arg290Gly
ENST00000537682.5:c.1501C>G	ENSP00000438611.1:p.Arg501Gly
ENST00000538326.5:c.*126C>G	ENSP00000437486.1:n.*126C>G
ENST00000539145.5:c.422C>G	ENSP00000444471.1:n.422C>G
ENST00000539154.1:n.866C>G
ENST00000541159.5:c.868C>G	ENSP00000438711.1:p.Arg290Gly
ENST00000542898.5:c.1594C>G	ENSP00000444615.1:p.Arg532Gly
ENST00000570511.5:c.1055C>G	ENSP00000458312.1:n.1055C>G
ENST00000572244.5:c.278-555C>G	ENSP00000461186.1:n.278-555C>G
ENST00000574583.5:c.422C>G	ENSP00000460269.1:n.422C>G
ENST00000576315.5:c.422C>G	ENSP00000460551.1:n.422C>G
ENST00000621655.1:c.868C>G	ENSP00000481436.1:p.Arg290Gly
NM_000243.2:c.1501C>G , LRG_190t1:c.1501C>G	NP_000234.1:p.Arg501Gly
NM_001198536.1:c.868C>G	NP_001185465.1:p.Arg290Gly
XM_017023236.2:c.1498C>G	XP_016878725.1:p.Arg500Gly
XR_001751903.1:n.1690C>G
NM_000243.3:c.1501C>G MANE Select	NP_000234.1:p.Arg501Gly
NM_001198536.2:c.868C>G	NP_001185465.2:p.Arg290Gly