Canonical Allele Identifier: CA2089999787

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48423402_48423403delinsAG , CM000675.2:g.48423402_48423403delinsAG GRCh38
NC_000013.10:g.48997538_48997539delinsAG , CM000675.1:g.48997538_48997539delinsAG GRCh37
NC_000013.9:g.47895539_47895540delinsAG NCBI36
NG_009009.1:g.124656_124657delinsAG , LRG_517:g.124656_124657delinsAG
NG_012874.1:g.26302_26303delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1696-29591_1696-29590delinsAG (RB1) MANE Select ENSP00000267163.4:n.1696-29591_1696-29590delinsAG
ENST00000643064.1:c.194+41959_194+41960delinsAG (RB1)
ENST00000650461.1:c.1696-29591_1696-29590delinsAG (RB1) ENSP00000497193.1:n.1696-29591_1696-29590delinsAG
ENST00000267163.4:c.1696-29591_1696-29590delinsAG (RB1) ENSP00000267163.4:n.1696-29591_1696-29590delinsAG
ENST00000345941.2:c.-1094-613_-1094-612delinsCT (LPAR6) ENSP00000344353.2:n.-1094-613_-1094-612delinsCT
ENST00000378434.8:c.-1347+590_-1347+591delinsCT (LPAR6) ENSP00000367691.3:n.-1347+590_-1347+591delinsCT
ENST00000465365.6:n.662+590_662+591delinsCT (LPAR6)
NM_000321.2:c.1696-29591_1696-29590delinsAG , LRG_517t1:c.1696-29591_1696-29590delinsAG (RB1) NP_000312.2:n.1696-29591_1696-29590delinsAG
NM_001162497.1:c.-1094-613_-1094-612delinsCT (LPAR6) NP_001155969.1:n.-1094-613_-1094-612delinsCT
NM_005767.5:c.-1347+590_-1347+591delinsCT (LPAR6) NP_005758.2:n.-1347+590_-1347+591delinsCT
XM_011535171.1:c.1435-29591_1435-29590delinsAG (RB1) XP_011533473.1:n.1435-29591_1435-29590delinsAG
XM_011535171.2:c.1435-29591_1435-29590delinsAG (RB1) XP_011533473.1:n.1435-29591_1435-29590delinsAG
NM_001162497.2:c.-1094-613_-1094-612delinsCT (LPAR6) NP_001155969.1:n.-1094-613_-1094-612delinsCT
NM_001377316.1:c.-1094-613_-1094-612delinsCT (LPAR6) NP_001364245.1:n.-1094-613_-1094-612delinsCT
NM_001377317.1:c.-1094-613_-1094-612delinsCT (LPAR6) NP_001364246.1:n.-1094-613_-1094-612delinsCT
NM_005767.6:c.-1347+590_-1347+591delinsCT (LPAR6) NP_005758.2:n.-1347+590_-1347+591delinsCT
NM_000321.3:c.1696-29591_1696-29590delinsAG (RB1) MANE Select NP_000312.2:n.1696-29591_1696-29590delinsAG
NM_001162497.3:c.-1094-613_-1094-612delinsCT (LPAR6) NP_001155969.1:n.-1094-613_-1094-612delinsCT
NM_001377316.2:c.-1094-613_-1094-612delinsCT (LPAR6) NP_001364245.1:n.-1094-613_-1094-612delinsCT
NM_001377317.2:c.-1094-613_-1094-612delinsCT (LPAR6) NP_001364246.1:n.-1094-613_-1094-612delinsCT
NM_005767.7:c.-1347+590_-1347+591delinsCT (LPAR6) NP_005758.2:n.-1347+590_-1347+591delinsCT