Canonical Allele Identifier: CA394484170

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293141T>C (hg19) ; chr16:g.3243141T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243141T>C , CM000678.2:g.3243141T>C	GRCh38
NC_000016.9:g.3293141T>C , CM000678.1:g.3293141T>C	GRCh37
NC_000016.8:g.3233142T>C	NCBI36
NG_007871.1:g.18487A>G , LRG_190:g.18487A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1467A>G
ENST00000219596.6:c.2346A>G MANE Select	ENSP00000219596.1:p.Ter782Trp
ENST00000219596.5:c.2346A>G	ENSP00000219596.1:p.Ter782Trp
ENST00000339854.8:c.1806A>G	ENSP00000339639.4:p.Ter602Trp
ENST00000536379.5:c.1713A>G	ENSP00000445079.1:p.Ter571Trp
ENST00000536980.5:c.*622A>G	ENSP00000444178.1:n.*622A>G
ENST00000537682.5:c.*622A>G	ENSP00000438611.1:n.*622A>G
ENST00000538326.5:c.*971A>G	ENSP00000437486.1:n.*971A>G
ENST00000539145.5:c.1267A>G	ENSP00000444471.1:n.1267A>G
ENST00000541159.5:c.1888A>G	ENSP00000438711.1:n.1888A>G
ENST00000542898.5:c.*622A>G	ENSP00000444615.1:n.*622A>G
ENST00000570511.5:c.1751A>G	ENSP00000458312.1:n.1751A>G
ENST00000572244.5:c.1036A>G	ENSP00000461186.1:n.1036A>G
ENST00000574583.5:c.1118A>G	ENSP00000460269.1:n.1118A>G
ENST00000576315.5:c.1151A>G	ENSP00000460551.1:n.1151A>G
ENST00000621655.1:c.1883A>G	ENSP00000481436.1:n.1883A>G
NM_000243.2:c.2346A>G , LRG_190t1:c.2346A>G	NP_000234.1:p.Ter782Trp
NM_001198536.1:c.*550A>G	NP_001185465.1:n.*550A>G
XM_017023236.2:c.2343A>G	XP_016878725.1:p.Ter781Trp
NM_000243.3:c.2346A>G MANE Select	NP_000234.1:p.Ter782Trp
NM_001198536.2:c.*550A>G	NP_001185465.2:n.*550A>G