Canonical Allele Identifier: CA280528

Gene: MEFV

Linked Data

• ClinVar Variation Id: 97495
• ClinVar RCV Id: RCV000083747
• dbSNP Id: rs104895145
• MyVariant Identifiers: chr16:g.3293374G>A (hg19) ; chr16:g.3243374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243374G>A , CM000678.2:g.3243374G>A	GRCh38
NC_000016.9:g.3293374G>A , CM000678.1:g.3293374G>A	GRCh37
NC_000016.8:g.3233375G>A	NCBI36
NG_007871.1:g.18254C>T , LRG_190:g.18254C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.1234C>T
ENST00000219596.6:c.2113C>T MANE Select	ENSP00000219596.1:p.Pro705Ser
ENST00000219596.5:c.2113C>T	ENSP00000219596.1:p.Pro705Ser
ENST00000339854.8:c.1573C>T	ENSP00000339639.4:p.Pro525Ser
ENST00000536379.5:c.1480C>T	ENSP00000445079.1:p.Pro494Ser
ENST00000536980.5:c.*389C>T	ENSP00000444178.1:n.*389C>T
ENST00000537682.5:c.*389C>T	ENSP00000438611.1:n.*389C>T
ENST00000538326.5:c.*738C>T	ENSP00000437486.1:n.*738C>T
ENST00000539145.5:c.1034C>T	ENSP00000444471.1:n.1034C>T
ENST00000541159.5:c.1655C>T	ENSP00000438711.1:n.1655C>T
ENST00000542898.5:c.*389C>T	ENSP00000444615.1:n.*389C>T
ENST00000570511.5:c.1518C>T	ENSP00000458312.1:n.1518C>T
ENST00000572244.5:c.803C>T	ENSP00000461186.1:n.803C>T
ENST00000574583.5:c.885C>T	ENSP00000460269.1:n.885C>T
ENST00000576315.5:c.918C>T	ENSP00000460551.1:n.918C>T
ENST00000621655.1:c.1650C>T	ENSP00000481436.1:n.1650C>T
NM_000243.2:c.2113C>T , LRG_190t1:c.2113C>T	NP_000234.1:p.Pro705Ser
NM_001198536.1:c.*317C>T	NP_001185465.1:n.*317C>T
XM_017023236.2:c.2110C>T	XP_016878725.1:p.Pro704Ser
NM_000243.3:c.2113C>T MANE Select	NP_000234.1:p.Pro705Ser
NM_001198536.2:c.*317C>T	NP_001185465.2:n.*317C>T