Canonical Allele Identifier: CA2736091170

Gene: NLRP7

Linked Data

• dbSNP Id: rs2146213980

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54939142_54939150del , CM000681.2:g.54939142_54939150del	GRCh38
NC_000019.8:g.60142322_60142330del	NCBI36
NG_008056.1:g.13356_13364del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592784.6:c.1669_1677del MANE Select	ENSP00000468706.1:p.Leu557_Ala559del
ENST00000328092.9:c.1669_1677del	ENSP00000329568.5:p.Leu557_Ala559del
ENST00000340844.6:c.1669_1677del	ENSP00000339491.2:p.Leu557_Ala559del
ENST00000586379.5:c.1669_1677del	ENSP00000468243.1:p.Leu557_Ala559del
ENST00000588756.5:c.1669_1677del	ENSP00000467123.1:p.Leu557_Ala559del
ENST00000590030.5:c.1669_1677del	ENSP00000465520.1:p.Leu557_Ala559del
ENST00000592784.5:c.1669_1677del	ENSP00000468706.1:p.Leu557_Ala559del
NM_001127255.1:c.1669_1677del	NP_001120727.1:p.Leu557_Ala559del
NM_139176.3:c.1669_1677del	NP_631915.2:p.Leu557_Ala559del
NM_206828.3:c.1669_1677del	NP_996611.2:p.Leu557_Ala559del
XM_006723075.2:c.1669_1677del	XP_006723138.1:p.Leu557_Ala559del
XM_006723076.2:c.1669_1677del	XP_006723139.1:p.Leu557_Ala559del
XM_011526596.1:c.1753_1761del	XP_011524898.1:p.Leu585_Ala587del
XM_011526597.1:c.1753_1761del	XP_011524899.1:p.Leu585_Ala587del
XM_011526598.1:c.1753_1761del	XP_011524900.1:p.Leu585_Ala587del
XM_011526599.1:c.1669_1677del	XP_011524901.1:p.Leu557_Ala559del
XM_011526600.1:c.1669_1677del	XP_011524902.1:p.Leu557_Ala559del
XM_011526601.1:c.1753_1761del	XP_011524903.1:p.Leu585_Ala587del
XR_935761.1:n.2187_2195del
XM_006723075.3:c.1669_1677del	XP_006723138.1:p.Leu557_Ala559del
XM_006723076.3:c.1669_1677del	XP_006723139.1:p.Leu557_Ala559del
XM_011526596.2:c.1753_1761del	XP_011524898.1:p.Leu585_Ala587del
XM_011526599.2:c.1669_1677del	XP_011524901.1:p.Leu557_Ala559del
XM_011526601.2:c.1753_1761del	XP_011524903.1:p.Leu585_Ala587del