Canonical Allele Identifier: CA394487615

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293557C>T (hg19) ; chr16:g.3243557C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243557C>T , CM000678.2:g.3243557C>T	GRCh38
NC_000016.9:g.3293557C>T , CM000678.1:g.3293557C>T	GRCh37
NC_000016.8:g.3233558C>T	NCBI36
NG_007871.1:g.18071G>A , LRG_190:g.18071G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1051G>A
ENST00000219596.6:c.1930G>A MANE Select	ENSP00000219596.1:p.Gly644Ser
ENST00000219596.5:c.1930G>A	ENSP00000219596.1:p.Gly644Ser
ENST00000339854.8:c.1390G>A	ENSP00000339639.4:p.Gly464Ser
ENST00000536379.5:c.1297G>A	ENSP00000445079.1:p.Gly433Ser
ENST00000536980.5:c.*206G>A	ENSP00000444178.1:n.*206G>A
ENST00000537682.5:c.*206G>A	ENSP00000438611.1:n.*206G>A
ENST00000538326.5:c.*555G>A	ENSP00000437486.1:n.*555G>A
ENST00000539145.5:c.851G>A	ENSP00000444471.1:n.851G>A
ENST00000541159.5:c.1472G>A	ENSP00000438711.1:n.1472G>A
ENST00000542898.5:c.*206G>A	ENSP00000444615.1:n.*206G>A
ENST00000570511.5:c.1335G>A	ENSP00000458312.1:n.1335G>A
ENST00000572244.5:c.620G>A	ENSP00000461186.1:n.620G>A
ENST00000574583.5:c.702G>A	ENSP00000460269.1:n.702G>A
ENST00000576315.5:c.735G>A	ENSP00000460551.1:n.735G>A
ENST00000621655.1:c.1467G>A	ENSP00000481436.1:n.1467G>A
NM_000243.2:c.1930G>A , LRG_190t1:c.1930G>A	NP_000234.1:p.Gly644Ser
NM_001198536.1:c.*134G>A	NP_001185465.1:n.*134G>A
XM_017023236.2:c.1927G>A	XP_016878725.1:p.Gly643Ser
NM_000243.3:c.1930G>A MANE Select	NP_000234.1:p.Gly644Ser
NM_001198536.2:c.*134G>A	NP_001185465.2:n.*134G>A