Canonical Allele Identifier: CA493383614

Gene: MEFV

Linked Data

• MyVariant Identifiers: chr16:g.3293297G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243297G>A , CM000678.2:g.3243297G>A	GRCh38
NC_000016.9:g.3293297G>A , CM000678.1:g.3293297G>A	GRCh37
NC_000016.8:g.3233298G>A	NCBI36
NG_007871.1:g.18331C>T , LRG_190:g.18331C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1311C>T
ENST00000219596.6:c.2190C>T MANE Select	ENSP00000219596.1:p.Ser730=
ENST00000219596.5:c.2190C>T	ENSP00000219596.1:p.Ser730=
ENST00000339854.8:c.1650C>T	ENSP00000339639.4:p.Ser550=
ENST00000536379.5:c.1557C>T	ENSP00000445079.1:p.Ser519=
ENST00000536980.5:c.*466C>T	ENSP00000444178.1:n.*466C>T
ENST00000537682.5:c.*466C>T	ENSP00000438611.1:n.*466C>T
ENST00000538326.5:c.*815C>T	ENSP00000437486.1:n.*815C>T
ENST00000539145.5:c.1111C>T	ENSP00000444471.1:n.1111C>T
ENST00000541159.5:c.1732C>T	ENSP00000438711.1:n.1732C>T
ENST00000542898.5:c.*466C>T	ENSP00000444615.1:n.*466C>T
ENST00000570511.5:c.1595C>T	ENSP00000458312.1:n.1595C>T
ENST00000572244.5:c.880C>T	ENSP00000461186.1:n.880C>T
ENST00000574583.5:c.962C>T	ENSP00000460269.1:n.962C>T
ENST00000576315.5:c.995C>T	ENSP00000460551.1:n.995C>T
ENST00000621655.1:c.1727C>T	ENSP00000481436.1:n.1727C>T
NM_000243.2:c.2190C>T , LRG_190t1:c.2190C>T	NP_000234.1:p.Ser730=
NM_001198536.1:c.*394C>T	NP_001185465.1:n.*394C>T
XM_017023236.2:c.2187C>T	XP_016878725.1:p.Ser729=
NM_000243.3:c.2190C>T MANE Select	NP_000234.1:p.Ser730=
NM_001198536.2:c.*394C>T	NP_001185465.2:n.*394C>T