Canonical Allele Identifier: CA2631334218

Gene: MEFV

Linked Data

• gnomAD v4: 16-3244411-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244411G>A , CM000678.2:g.3244411G>A	GRCh38
NC_000016.9:g.3294411G>A , CM000678.1:g.3294411G>A	GRCh37
NC_000016.8:g.3234412G>A	NCBI36
NG_007871.1:g.17217C>T , LRG_190:g.17217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.847+62C>T
ENST00000219596.6:c.1726+62C>T MANE Select	ENSP00000219596.1:n.1726+62C>T
ENST00000219596.5:c.1726+62C>T	ENSP00000219596.1:n.1726+62C>T
ENST00000339854.8:c.1186+62C>T	ENSP00000339639.4:n.1186+62C>T
ENST00000536379.5:c.1093+62C>T	ENSP00000445079.1:n.1093+62C>T
ENST00000536980.5:c.1093+62C>T	ENSP00000444178.1:n.1093+62C>T
ENST00000537682.5:c.1726+62C>T	ENSP00000438611.1:n.1726+62C>T
ENST00000538326.5:c.*351+62C>T	ENSP00000437486.1:n.*351+62C>T
ENST00000539145.5:c.647+62C>T	ENSP00000444471.1:n.647+62C>T
ENST00000541159.5:c.1093+62C>T	ENSP00000438711.1:n.1093+62C>T
ENST00000542898.5:c.1819+62C>T	ENSP00000444615.1:n.1819+62C>T
ENST00000570511.5:c.1165-519C>T	ENSP00000458312.1:n.1165-519C>T
ENST00000572244.5:c.416+62C>T	ENSP00000461186.1:n.416+62C>T
ENST00000574583.5:c.532-519C>T	ENSP00000460269.1:n.532-519C>T
ENST00000576315.5:c.532-125C>T	ENSP00000460551.1:n.532-125C>T
ENST00000621655.1:c.1093+62C>T	ENSP00000481436.1:n.1093+62C>T
NM_000243.2:c.1726+62C>T , LRG_190t1:c.1726+62C>T	NP_000234.1:n.1726+62C>T
NM_001198536.1:c.1093+62C>T	NP_001185465.1:n.1093+62C>T
XM_017023236.2:c.1723+62C>T	XP_016878725.1:n.1723+62C>T
XR_001751903.1:n.1915+62C>T
NM_000243.3:c.1726+62C>T MANE Select	NP_000234.1:n.1726+62C>T
NM_001198536.2:c.1093+62C>T	NP_001185465.2:n.1093+62C>T