Canonical Allele Identifier: CA394457813

Gene: MEFV

Linked Data

• gnomAD v4: 16-3244482-A-T
• MyVariant Identifiers: chr16:g.3294482A>T (hg19) ; chr16:g.3244482A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244482A>T , CM000678.2:g.3244482A>T	GRCh38
NC_000016.9:g.3294482A>T , CM000678.1:g.3294482A>T	GRCh37
NC_000016.8:g.3234483A>T	NCBI36
NG_007871.1:g.17146T>A , LRG_190:g.17146T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.838T>A
ENST00000219596.6:c.1717T>A MANE Select	ENSP00000219596.1:p.Tyr573Asn
ENST00000219596.5:c.1717T>A	ENSP00000219596.1:p.Tyr573Asn
ENST00000339854.8:c.1177T>A	ENSP00000339639.4:p.Tyr393Asn
ENST00000536379.5:c.1084T>A	ENSP00000445079.1:p.Tyr362Asn
ENST00000536980.5:c.1084T>A	ENSP00000444178.1:p.Tyr362Asn
ENST00000537682.5:c.1717T>A	ENSP00000438611.1:p.Tyr573Asn
ENST00000538326.5:c.*342T>A	ENSP00000437486.1:n.*342T>A
ENST00000539145.5:c.638T>A	ENSP00000444471.1:n.638T>A
ENST00000541159.5:c.1084T>A	ENSP00000438711.1:p.Tyr362Asn
ENST00000542898.5:c.1810T>A	ENSP00000444615.1:p.Tyr604Asn
ENST00000570511.5:c.1165-590T>A	ENSP00000458312.1:n.1165-590T>A
ENST00000572244.5:c.407T>A	ENSP00000461186.1:n.407T>A
ENST00000574583.5:c.532-590T>A	ENSP00000460269.1:n.532-590T>A
ENST00000576315.5:c.532-196T>A	ENSP00000460551.1:n.532-196T>A
ENST00000621655.1:c.1084T>A	ENSP00000481436.1:p.Tyr362Asn
NM_000243.2:c.1717T>A , LRG_190t1:c.1717T>A	NP_000234.1:p.Tyr573Asn
NM_001198536.1:c.1084T>A	NP_001185465.1:p.Tyr362Asn
XM_017023236.2:c.1714T>A	XP_016878725.1:p.Tyr572Asn
XR_001751903.1:n.1906T>A
NM_000243.3:c.1717T>A MANE Select	NP_000234.1:p.Tyr573Asn
NM_001198536.2:c.1084T>A	NP_001185465.2:p.Tyr362Asn