Canonical Allele Identifier: CA394487735

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293575T>G (hg19) ; chr16:g.3243575T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243575T>G , CM000678.2:g.3243575T>G	GRCh38
NC_000016.9:g.3293575T>G , CM000678.1:g.3293575T>G	GRCh37
NC_000016.8:g.3233576T>G	NCBI36
NG_007871.1:g.18053A>C , LRG_190:g.18053A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1033A>C
ENST00000219596.6:c.1912A>C MANE Select	ENSP00000219596.1:p.Ser638Arg
ENST00000219596.5:c.1912A>C	ENSP00000219596.1:p.Ser638Arg
ENST00000339854.8:c.1372A>C	ENSP00000339639.4:p.Ser458Arg
ENST00000536379.5:c.1279A>C	ENSP00000445079.1:p.Ser427Arg
ENST00000536980.5:c.*188A>C	ENSP00000444178.1:n.*188A>C
ENST00000537682.5:c.*188A>C	ENSP00000438611.1:n.*188A>C
ENST00000538326.5:c.*537A>C	ENSP00000437486.1:n.*537A>C
ENST00000539145.5:c.833A>C	ENSP00000444471.1:n.833A>C
ENST00000541159.5:c.1454A>C	ENSP00000438711.1:n.1454A>C
ENST00000542898.5:c.*188A>C	ENSP00000444615.1:n.*188A>C
ENST00000570511.5:c.1317A>C	ENSP00000458312.1:n.1317A>C
ENST00000572244.5:c.602A>C	ENSP00000461186.1:n.602A>C
ENST00000574583.5:c.684A>C	ENSP00000460269.1:n.684A>C
ENST00000576315.5:c.717A>C	ENSP00000460551.1:n.717A>C
ENST00000621655.1:c.1449A>C	ENSP00000481436.1:n.1449A>C
NM_000243.2:c.1912A>C , LRG_190t1:c.1912A>C	NP_000234.1:p.Ser638Arg
NM_001198536.1:c.*116A>C	NP_001185465.1:n.*116A>C
XM_017023236.2:c.1909A>C	XP_016878725.1:p.Ser637Arg
NM_000243.3:c.1912A>C MANE Select	NP_000234.1:p.Ser638Arg
NM_001198536.2:c.*116A>C	NP_001185465.2:n.*116A>C