Canonical Allele Identifier: CA394485902

Gene: MEFV

Linked Data

• gnomAD v4: 16-3243374-G-C
• MyVariant Identifiers: chr16:g.3293374G>C (hg19) ; chr16:g.3243374G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1234C>G
ENST00000219596.6:c.2113C>G MANE Select	ENSP00000219596.1:p.Pro705Ala
ENST00000219596.5:c.2113C>G	ENSP00000219596.1:p.Pro705Ala
ENST00000339854.8:c.1573C>G	ENSP00000339639.4:p.Pro525Ala
ENST00000536379.5:c.1480C>G	ENSP00000445079.1:p.Pro494Ala
ENST00000536980.5:c.*389C>G	ENSP00000444178.1:n.*389C>G
ENST00000537682.5:c.*389C>G	ENSP00000438611.1:n.*389C>G
ENST00000538326.5:c.*738C>G	ENSP00000437486.1:n.*738C>G
ENST00000539145.5:c.1034C>G	ENSP00000444471.1:n.1034C>G
ENST00000541159.5:c.1655C>G	ENSP00000438711.1:n.1655C>G
ENST00000542898.5:c.*389C>G	ENSP00000444615.1:n.*389C>G
ENST00000570511.5:c.1518C>G	ENSP00000458312.1:n.1518C>G
ENST00000572244.5:c.803C>G	ENSP00000461186.1:n.803C>G
ENST00000574583.5:c.885C>G	ENSP00000460269.1:n.885C>G
ENST00000576315.5:c.918C>G	ENSP00000460551.1:n.918C>G
ENST00000621655.1:c.1650C>G	ENSP00000481436.1:n.1650C>G
NM_000243.2:c.2113C>G , LRG_190t1:c.2113C>G	NP_000234.1:p.Pro705Ala
NM_001198536.1:c.*317C>G	NP_001185465.1:n.*317C>G
XM_017023236.2:c.2110C>G	XP_016878725.1:p.Pro704Ala
NM_000243.3:c.2113C>G MANE Select	NP_000234.1:p.Pro705Ala
NM_001198536.2:c.*317C>G	NP_001185465.2:n.*317C>G