Canonical Allele Identifier: CA394486329

Gene: MEFV

Linked Data

• gnomAD v4: 16-3243424-T-G
• MyVariant Identifiers: chr16:g.3293424T>G (hg19) ; chr16:g.3243424T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243424T>G , CM000678.2:g.3243424T>G	GRCh38
NC_000016.9:g.3293424T>G , CM000678.1:g.3293424T>G	GRCh37
NC_000016.8:g.3233425T>G	NCBI36
NG_007871.1:g.18204A>C , LRG_190:g.18204A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1184A>C
ENST00000219596.6:c.2063A>C MANE Select	ENSP00000219596.1:p.Tyr688Ser
ENST00000219596.5:c.2063A>C	ENSP00000219596.1:p.Tyr688Ser
ENST00000339854.8:c.1523A>C	ENSP00000339639.4:p.Tyr508Ser
ENST00000536379.5:c.1430A>C	ENSP00000445079.1:p.Tyr477Ser
ENST00000536980.5:c.*339A>C	ENSP00000444178.1:n.*339A>C
ENST00000537682.5:c.*339A>C	ENSP00000438611.1:n.*339A>C
ENST00000538326.5:c.*688A>C	ENSP00000437486.1:n.*688A>C
ENST00000539145.5:c.984A>C	ENSP00000444471.1:n.984A>C
ENST00000541159.5:c.1605A>C	ENSP00000438711.1:n.1605A>C
ENST00000542898.5:c.*339A>C	ENSP00000444615.1:n.*339A>C
ENST00000570511.5:c.1468A>C	ENSP00000458312.1:n.1468A>C
ENST00000572244.5:c.753A>C	ENSP00000461186.1:n.753A>C
ENST00000574583.5:c.835A>C	ENSP00000460269.1:n.835A>C
ENST00000576315.5:c.868A>C	ENSP00000460551.1:n.868A>C
ENST00000621655.1:c.1600A>C	ENSP00000481436.1:n.1600A>C
NM_000243.2:c.2063A>C , LRG_190t1:c.2063A>C	NP_000234.1:p.Tyr688Ser
NM_001198536.1:c.*267A>C	NP_001185465.1:n.*267A>C
XM_017023236.2:c.2060A>C	XP_016878725.1:p.Tyr687Ser
NM_000243.3:c.2063A>C MANE Select	NP_000234.1:p.Tyr688Ser
NM_001198536.2:c.*267A>C	NP_001185465.2:n.*267A>C