Canonical Allele Identifier: CA720025884

Gene: MEFV

Linked Data

• dbSNP Id: rs1474821428
• gnomAD v3: 16-3244218-C-T
• gnomAD v4: 16-3244218-C-T
• MyVariant Identifiers: chr16:g.3294218C>T (hg19) ; chr16:g.3244218C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244218C>T , CM000678.2:g.3244218C>T	GRCh38
NC_000016.9:g.3294218C>T , CM000678.1:g.3294218C>T	GRCh37
NC_000016.8:g.3234219C>T	NCBI36
NG_007871.1:g.17410G>A , LRG_190:g.17410G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697124.1:n.880+36G>A
ENST00000219596.6:c.1759+36G>A MANE Select	ENSP00000219596.1:n.1759+36G>A
ENST00000219596.5:c.1759+36G>A	ENSP00000219596.1:n.1759+36G>A
ENST00000339854.8:c.1219+36G>A	ENSP00000339639.4:n.1219+36G>A
ENST00000536379.5:c.1126+36G>A	ENSP00000445079.1:n.1126+36G>A
ENST00000536980.5:c.1162G>A	ENSP00000444178.1:p.Val388Ile
ENST00000537682.5:c.1795G>A	ENSP00000438611.1:p.Val599Ile
ENST00000538326.5:c.*384+36G>A	ENSP00000437486.1:n.*384+36G>A
ENST00000539145.5:c.680+36G>A	ENSP00000444471.1:n.680+36G>A
ENST00000541159.5:c.1126+36G>A	ENSP00000438711.1:n.1126+36G>A
ENST00000542898.5:c.1888G>A	ENSP00000444615.1:p.Val630Ile
ENST00000570511.5:c.1165-326G>A	ENSP00000458312.1:n.1165-326G>A
ENST00000572244.5:c.449+36G>A	ENSP00000461186.1:n.449+36G>A
ENST00000574583.5:c.532-326G>A	ENSP00000460269.1:n.532-326G>A
ENST00000576315.5:c.564+36G>A	ENSP00000460551.1:n.564+36G>A
ENST00000621655.1:c.1126+36G>A	ENSP00000481436.1:n.1126+36G>A
NM_000243.2:c.1759+36G>A , LRG_190t1:c.1759+36G>A	NP_000234.1:n.1759+36G>A
NM_001198536.1:c.1126+36G>A	NP_001185465.1:n.1126+36G>A
XM_017023236.2:c.1756+36G>A	XP_016878725.1:n.1756+36G>A
XR_001751903.1:n.1984G>A
NM_000243.3:c.1759+36G>A MANE Select	NP_000234.1:n.1759+36G>A
NM_001198536.2:c.1126+36G>A	NP_001185465.2:n.1126+36G>A