Canonical Allele Identifier: CA2631333997

Gene: MEFV

Linked Data

• gnomAD v4: 16-3243734-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243735del , CM000678.2:g.3243735del	GRCh38
NC_000016.9:g.3293735del , CM000678.1:g.3293735del	GRCh37
NC_000016.8:g.3233736del	NCBI36
NG_007871.1:g.17893del , LRG_190:g.17893del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.914-41del
ENST00000219596.6:c.1793-41del MANE Select	ENSP00000219596.1:n.1793-41del
ENST00000219596.5:c.1793-41del	ENSP00000219596.1:n.1793-41del
ENST00000339854.8:c.1253-41del	ENSP00000339639.4:n.1253-41del
ENST00000536379.5:c.1160-41del	ENSP00000445079.1:n.1160-41del
ENST00000536980.5:c.*69-41del	ENSP00000444178.1:n.*69-41del
ENST00000537682.5:c.*69-41del	ENSP00000438611.1:n.*69-41del
ENST00000538326.5:c.*418-41del	ENSP00000437486.1:n.*418-41del
ENST00000539145.5:c.714-41del	ENSP00000444471.1:n.714-41del
ENST00000541159.5:c.1335-41del	ENSP00000438711.1:n.1335-41del
ENST00000542898.5:c.*69-41del	ENSP00000444615.1:n.*69-41del
ENST00000570511.5:c.1198-41del	ENSP00000458312.1:n.1198-41del
ENST00000572244.5:c.483-41del	ENSP00000461186.1:n.483-41del
ENST00000574583.5:c.565-41del	ENSP00000460269.1:n.565-41del
ENST00000576315.5:c.598-41del	ENSP00000460551.1:n.598-41del
ENST00000621655.1:c.1330-41del	ENSP00000481436.1:n.1330-41del
NM_000243.2:c.1793-41del , LRG_190t1:c.1793-41del	NP_000234.1:n.1793-41del
NM_001198536.1:c.1335-41del	NP_001185465.1:n.1335-41del
XM_017023236.2:c.1790-41del	XP_016878725.1:n.1790-41del
XR_001751903.1:n.2100-41del
NM_000243.3:c.1793-41del MANE Select	NP_000234.1:n.1793-41del
NM_001198536.2:c.1335-41del	NP_001185465.2:n.1335-41del