Canonical Allele Identifier: CA394486025

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293393C>G (hg19) ; chr16:g.3243393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243393C>G , CM000678.2:g.3243393C>G	GRCh38
NC_000016.9:g.3293393C>G , CM000678.1:g.3293393C>G	GRCh37
NC_000016.8:g.3233394C>G	NCBI36
NG_007871.1:g.18235G>C , LRG_190:g.18235G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1215G>C
ENST00000219596.6:c.2094G>C MANE Select	ENSP00000219596.1:p.Glu698Asp
ENST00000219596.5:c.2094G>C	ENSP00000219596.1:p.Glu698Asp
ENST00000339854.8:c.1554G>C	ENSP00000339639.4:p.Glu518Asp
ENST00000536379.5:c.1461G>C	ENSP00000445079.1:p.Glu487Asp
ENST00000536980.5:c.*370G>C	ENSP00000444178.1:n.*370G>C
ENST00000537682.5:c.*370G>C	ENSP00000438611.1:n.*370G>C
ENST00000538326.5:c.*719G>C	ENSP00000437486.1:n.*719G>C
ENST00000539145.5:c.1015G>C	ENSP00000444471.1:n.1015G>C
ENST00000541159.5:c.1636G>C	ENSP00000438711.1:n.1636G>C
ENST00000542898.5:c.*370G>C	ENSP00000444615.1:n.*370G>C
ENST00000570511.5:c.1499G>C	ENSP00000458312.1:n.1499G>C
ENST00000572244.5:c.784G>C	ENSP00000461186.1:n.784G>C
ENST00000574583.5:c.866G>C	ENSP00000460269.1:n.866G>C
ENST00000576315.5:c.899G>C	ENSP00000460551.1:n.899G>C
ENST00000621655.1:c.1631G>C	ENSP00000481436.1:n.1631G>C
NM_000243.2:c.2094G>C , LRG_190t1:c.2094G>C	NP_000234.1:p.Glu698Asp
NM_001198536.1:c.*298G>C	NP_001185465.1:n.*298G>C
XM_017023236.2:c.2091G>C	XP_016878725.1:p.Glu697Asp
NM_000243.3:c.2094G>C MANE Select	NP_000234.1:p.Glu698Asp
NM_001198536.2:c.*298G>C	NP_001185465.2:n.*298G>C