Canonical Allele Identifier: CA276899102

Gene: MEFV

Linked Data

• ClinVar Variation Id: 1209626
• ClinVar RCV Id: RCV001578714
• dbSNP Id: rs906390314
• MyVariant Identifiers: chr16:g.3299775G>A (hg19) ; chr16:g.3249775G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3249775G>A , CM000678.2:g.3249775G>A	GRCh38
NC_000016.9:g.3299775G>A , CM000678.1:g.3299775G>A	GRCh37
NC_000016.8:g.3239776G>A	NCBI36
NG_007871.1:g.11853C>T , LRG_190:g.11853C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219596.6:c.916C>T MANE Select	ENSP00000219596.1:p.Pro306Ser
ENST00000219596.5:c.916C>T	ENSP00000219596.1:p.Pro306Ser
ENST00000339854.8:c.376C>T	ENSP00000339639.4:p.Pro126Ser
ENST00000536379.5:c.283C>T	ENSP00000445079.1:p.Pro95Ser
ENST00000536980.5:c.283C>T	ENSP00000444178.1:p.Pro95Ser
ENST00000537682.5:c.916C>T	ENSP00000438611.1:p.Pro306Ser
ENST00000538326.5:c.916C>T	ENSP00000437486.1:p.Pro306Ser
ENST00000539145.5:c.278-2529C>T	ENSP00000444471.1:n.278-2529C>T
ENST00000541159.5:c.283C>T	ENSP00000438711.1:p.Pro95Ser
ENST00000542898.5:c.1009C>T	ENSP00000444615.1:p.Pro337Ser
ENST00000570511.5:c.911-2529C>T	ENSP00000458312.1:n.911-2529C>T
ENST00000572244.5:c.278-3228C>T	ENSP00000461186.1:n.278-3228C>T
ENST00000574583.5:c.278-2529C>T	ENSP00000460269.1:n.278-2529C>T
ENST00000576315.5:c.278-2529C>T	ENSP00000460551.1:n.278-2529C>T
ENST00000621655.1:c.283C>T	ENSP00000481436.1:p.Pro95Ser
NM_000243.2:c.916C>T , LRG_190t1:c.916C>T	NP_000234.1:p.Pro306Ser
NM_001198536.1:c.283C>T	NP_001185465.1:p.Pro95Ser
XM_017023236.2:c.916C>T	XP_016878725.1:p.Pro306Ser
XR_001751903.1:n.1105C>T
NM_000243.3:c.916C>T MANE Select	NP_000234.1:p.Pro306Ser
NM_001198536.2:c.283C>T	NP_001185465.2:p.Pro95Ser