Canonical Allele Identifier: CA2343162532

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54961534_54961535delinsAT , CM000681.2:g.54961534_54961535delinsAT GRCh38
NC_000019.8:g.60164714_60164715delinsAT NCBI36
NG_052633.1:g.13405_13406delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000587103.5:c.-77+4505_-77+4506delinsAT (NLRP7) ENSP00000467234.1:n.-77+4505_-77+4506delinsAT
ENST00000587844.1:c.-40+4505_-40+4506delinsAT (NLRP7) ENSP00000468161.1:n.-40+4505_-40+4506delinsAT
ENST00000588107.5:c.-18+8165_-18+8166delinsAT (NLRP2) ENSP00000465069.1:n.-18+8165_-18+8166delinsAT
ENST00000588619.5:c.-18+8249_-18+8250delinsAT (NLRP2) ENSP00000466260.1:n.-18+8249_-18+8250delinsAT
ENST00000588756.5:c.-284+4505_-284+4506delinsAT (NLRP7) ENSP00000467123.1:n.-284+4505_-284+4506delinsAT
ENST00000590659.1:c.-204+4505_-204+4506delinsAT (NLRP7) ENSP00000467589.1:n.-204+4505_-204+4506delinsAT
XM_006723075.2:c.-77+3415_-77+3416delinsAT (NLRP7) XP_006723138.1:n.-77+3415_-77+3416delinsAT
XM_006723076.2:c.-40+3415_-40+3416delinsAT (NLRP7) XP_006723139.1:n.-40+3415_-40+3416delinsAT
XM_011526596.1:c.-200+3415_-200+3416delinsAT (NLRP7) XP_011524898.1:n.-200+3415_-200+3416delinsAT
XM_011526597.1:c.-200+8321_-200+8322delinsAT (NLRP7) XP_011524899.1:n.-200+8321_-200+8322delinsAT
XM_011526598.1:c.-109+3415_-109+3416delinsAT (NLRP7) XP_011524900.1:n.-109+3415_-109+3416delinsAT
XM_011526599.1:c.-295+3415_-295+3416delinsAT (NLRP7) XP_011524901.1:n.-295+3415_-295+3416delinsAT
XM_011526600.1:c.-77+4505_-77+4506delinsAT (NLRP7) XP_011524902.1:n.-77+4505_-77+4506delinsAT
XM_011526601.1:c.-200+3415_-200+3416delinsAT (NLRP7) XP_011524903.1:n.-200+3415_-200+3416delinsAT
XR_935761.1:n.235+3415_235+3416delinsAT (NLRP7)
XM_006723075.3:c.-77+3415_-77+3416delinsAT (NLRP7) XP_006723138.1:n.-77+3415_-77+3416delinsAT
XM_006723076.3:c.-40+3415_-40+3416delinsAT (NLRP7) XP_006723139.1:n.-40+3415_-40+3416delinsAT
XM_011526596.2:c.-200+3415_-200+3416delinsAT (NLRP7) XP_011524898.1:n.-200+3415_-200+3416delinsAT
XM_011526599.2:c.-295+3415_-295+3416delinsAT (NLRP7) XP_011524901.1:n.-295+3415_-295+3416delinsAT
XM_011526601.2:c.-200+3415_-200+3416delinsAT (NLRP7) XP_011524903.1:n.-200+3415_-200+3416delinsAT