Canonical Allele Identifier: CA310042355

Linked Data

dbSNP Id: rs544604816

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54961515_54961522del , CM000681.2:g.54961515_54961522del GRCh38
NC_000019.8:g.60164695_60164702del NCBI36
NG_052633.1:g.13386_13393del

Transcript Alleles

HGVS Amino-acid change
ENST00000587103.5:c.-77+4534_-77+4541del (NLRP7) ENSP00000467234.1:n.-77+4534_-77+4541del
ENST00000587844.1:c.-40+4534_-40+4541del (NLRP7) ENSP00000468161.1:n.-40+4534_-40+4541del
ENST00000588107.5:c.-18+8146_-18+8153del (NLRP2) ENSP00000465069.1:n.-18+8146_-18+8153del
ENST00000588619.5:c.-18+8230_-18+8237del (NLRP2) ENSP00000466260.1:n.-18+8230_-18+8237del
ENST00000588756.5:c.-284+4534_-284+4541del (NLRP7) ENSP00000467123.1:n.-284+4534_-284+4541de...
ENST00000590659.1:c.-204+4534_-204+4541del (NLRP7) ENSP00000467589.1:n.-204+4534_-204+4541de...
XM_006723075.2:c.-77+3444_-77+3451del (NLRP7) XP_006723138.1:n.-77+3444_-77+3451del
XM_006723076.2:c.-40+3444_-40+3451del (NLRP7) XP_006723139.1:n.-40+3444_-40+3451del
XM_011526596.1:c.-200+3444_-200+3451del (NLRP7) XP_011524898.1:n.-200+3444_-200+3451del
XM_011526597.1:c.-200+8350_-200+8357del (NLRP7) XP_011524899.1:n.-200+8350_-200+8357del
XM_011526598.1:c.-109+3444_-109+3451del (NLRP7) XP_011524900.1:n.-109+3444_-109+3451del
XM_011526599.1:c.-295+3444_-295+3451del (NLRP7) XP_011524901.1:n.-295+3444_-295+3451del
XM_011526600.1:c.-77+4534_-77+4541del (NLRP7) XP_011524902.1:n.-77+4534_-77+4541del
XM_011526601.1:c.-200+3444_-200+3451del (NLRP7) XP_011524903.1:n.-200+3444_-200+3451del
XR_935761.1:n.235+3444_235+3451del (NLRP7)
XM_006723075.3:c.-77+3444_-77+3451del (NLRP7) XP_006723138.1:n.-77+3444_-77+3451del
XM_006723076.3:c.-40+3444_-40+3451del (NLRP7) XP_006723139.1:n.-40+3444_-40+3451del
XM_011526596.2:c.-200+3444_-200+3451del (NLRP7) XP_011524898.1:n.-200+3444_-200+3451del
XM_011526599.2:c.-295+3444_-295+3451del (NLRP7) XP_011524901.1:n.-295+3444_-295+3451del
XM_011526601.2:c.-200+3444_-200+3451del (NLRP7) XP_011524903.1:n.-200+3444_-200+3451del