Canonical Allele Identifier: CA2343162496

Gene: NLRP7 NLRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54961482_54961484delinsCAG , CM000681.2:g.54961482_54961484delinsCAG	GRCh38
NC_000019.8:g.60164662_60164664delinsCAG	NCBI36
NG_052633.1:g.13353_13355delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000587103.5:c.-77+4556_-77+4558delinsCTG (NLRP7)	ENSP00000467234.1:n.-77+4556_-77+4558deli...
ENST00000587844.1:c.-40+4556_-40+4558delinsCTG (NLRP7)	ENSP00000468161.1:n.-40+4556_-40+4558deli...
ENST00000588107.5:c.-18+8113_-18+8115delinsCAG (NLRP2)	ENSP00000465069.1:n.-18+8113_-18+8115deli...
ENST00000588619.5:c.-18+8197_-18+8199delinsCAG (NLRP2)	ENSP00000466260.1:n.-18+8197_-18+8199deli...
ENST00000588756.5:c.-284+4556_-284+4558delinsCTG (NLRP7)	ENSP00000467123.1:n.-284+4556_-284+4558de...
ENST00000590659.1:c.-204+4556_-204+4558delinsCTG (NLRP7)	ENSP00000467589.1:n.-204+4556_-204+4558de...
XM_006723075.2:c.-77+3466_-77+3468delinsCTG (NLRP7)	XP_006723138.1:n.-77+3466_-77+3468delinsC...
XM_006723076.2:c.-40+3466_-40+3468delinsCTG (NLRP7)	XP_006723139.1:n.-40+3466_-40+3468delinsC...
XM_011526596.1:c.-200+3466_-200+3468delinsCTG (NLRP7)	XP_011524898.1:n.-200+3466_-200+3468delin...
XM_011526597.1:c.-200+8372_-200+8374delinsCTG (NLRP7)	XP_011524899.1:n.-200+8372_-200+8374delin...
XM_011526598.1:c.-109+3466_-109+3468delinsCTG (NLRP7)	XP_011524900.1:n.-109+3466_-109+3468delin...
XM_011526599.1:c.-295+3466_-295+3468delinsCTG (NLRP7)	XP_011524901.1:n.-295+3466_-295+3468delin...
XM_011526600.1:c.-77+4556_-77+4558delinsCTG (NLRP7)	XP_011524902.1:n.-77+4556_-77+4558delinsC...
XM_011526601.1:c.-200+3466_-200+3468delinsCTG (NLRP7)	XP_011524903.1:n.-200+3466_-200+3468delin...
XR_935761.1:n.235+3466_235+3468delinsCTG (NLRP7)
XM_006723075.3:c.-77+3466_-77+3468delinsCTG (NLRP7)	XP_006723138.1:n.-77+3466_-77+3468delinsC...
XM_006723076.3:c.-40+3466_-40+3468delinsCTG (NLRP7)	XP_006723139.1:n.-40+3466_-40+3468delinsC...
XM_011526596.2:c.-200+3466_-200+3468delinsCTG (NLRP7)	XP_011524898.1:n.-200+3466_-200+3468delin...
XM_011526599.2:c.-295+3466_-295+3468delinsCTG (NLRP7)	XP_011524901.1:n.-295+3466_-295+3468delin...
XM_011526601.2:c.-200+3466_-200+3468delinsCTG (NLRP7)	XP_011524903.1:n.-200+3466_-200+3468delin...