Canonical Allele Identifier: CA394484351

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293167G>T (hg19) ; chr16:g.3243167G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243167G>T , CM000678.2:g.3243167G>T	GRCh38
NC_000016.9:g.3293167G>T , CM000678.1:g.3293167G>T	GRCh37
NC_000016.8:g.3233168G>T	NCBI36
NG_007871.1:g.18461C>A , LRG_190:g.18461C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1441C>A
ENST00000219596.6:c.2320C>A MANE Select	ENSP00000219596.1:p.Pro774Thr
ENST00000219596.5:c.2320C>A	ENSP00000219596.1:p.Pro774Thr
ENST00000339854.8:c.1780C>A	ENSP00000339639.4:p.Pro594Thr
ENST00000536379.5:c.1687C>A	ENSP00000445079.1:p.Pro563Thr
ENST00000536980.5:c.*596C>A	ENSP00000444178.1:n.*596C>A
ENST00000537682.5:c.*596C>A	ENSP00000438611.1:n.*596C>A
ENST00000538326.5:c.*945C>A	ENSP00000437486.1:n.*945C>A
ENST00000539145.5:c.1241C>A	ENSP00000444471.1:n.1241C>A
ENST00000541159.5:c.1862C>A	ENSP00000438711.1:n.1862C>A
ENST00000542898.5:c.*596C>A	ENSP00000444615.1:n.*596C>A
ENST00000570511.5:c.1725C>A	ENSP00000458312.1:n.1725C>A
ENST00000572244.5:c.1010C>A	ENSP00000461186.1:n.1010C>A
ENST00000574583.5:c.1092C>A	ENSP00000460269.1:n.1092C>A
ENST00000576315.5:c.1125C>A	ENSP00000460551.1:n.1125C>A
ENST00000621655.1:c.1857C>A	ENSP00000481436.1:n.1857C>A
NM_000243.2:c.2320C>A , LRG_190t1:c.2320C>A	NP_000234.1:p.Pro774Thr
NM_001198536.1:c.*524C>A	NP_001185465.1:n.*524C>A
XM_017023236.2:c.2317C>A	XP_016878725.1:p.Pro773Thr
NM_000243.3:c.2320C>A MANE Select	NP_000234.1:p.Pro774Thr
NM_001198536.2:c.*524C>A	NP_001185465.2:n.*524C>A