Canonical Allele Identifier: CA2089999769

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48423370_48423371delinsGT , CM000675.2:g.48423370_48423371delinsGT GRCh38
NC_000013.10:g.48997506_48997507delinsGT , CM000675.1:g.48997506_48997507delinsGT GRCh37
NC_000013.9:g.47895507_47895508delinsGT NCBI36
NG_009009.1:g.124624_124625delinsGT , LRG_517:g.124624_124625delinsGT
NG_012874.1:g.26334_26335delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1696-29623_1696-29622delinsGT (RB1) MANE Select ENSP00000267163.4:n.1696-29623_1696-29622delinsGT
ENST00000643064.1:c.194+41927_194+41928delinsGT (RB1)
ENST00000650461.1:c.1696-29623_1696-29622delinsGT (RB1) ENSP00000497193.1:n.1696-29623_1696-29622delinsGT
ENST00000267163.4:c.1696-29623_1696-29622delinsGT (RB1) ENSP00000267163.4:n.1696-29623_1696-29622delinsGT
ENST00000345941.2:c.-1094-581_-1094-580delinsAC (LPAR6) ENSP00000344353.2:n.-1094-581_-1094-580delinsAC
ENST00000378434.8:c.-1346-581_-1346-580delinsAC (LPAR6) ENSP00000367691.3:n.-1346-581_-1346-580delinsAC
ENST00000465365.6:n.663-581_663-580delinsAC (LPAR6)
NM_000321.2:c.1696-29623_1696-29622delinsGT , LRG_517t1:c.1696-29623_1696-29622delinsGT (RB1) NP_000312.2:n.1696-29623_1696-29622delinsGT
NM_001162497.1:c.-1094-581_-1094-580delinsAC (LPAR6) NP_001155969.1:n.-1094-581_-1094-580delinsAC
NM_005767.5:c.-1346-581_-1346-580delinsAC (LPAR6) NP_005758.2:n.-1346-581_-1346-580delinsAC
XM_011535171.1:c.1435-29623_1435-29622delinsGT (RB1) XP_011533473.1:n.1435-29623_1435-29622delinsGT
XM_011535171.2:c.1435-29623_1435-29622delinsGT (RB1) XP_011533473.1:n.1435-29623_1435-29622delinsGT
NM_001162497.2:c.-1094-581_-1094-580delinsAC (LPAR6) NP_001155969.1:n.-1094-581_-1094-580delinsAC
NM_001377316.1:c.-1094-581_-1094-580delinsAC (LPAR6) NP_001364245.1:n.-1094-581_-1094-580delinsAC
NM_001377317.1:c.-1094-581_-1094-580delinsAC (LPAR6) NP_001364246.1:n.-1094-581_-1094-580delinsAC
NM_005767.6:c.-1346-581_-1346-580delinsAC (LPAR6) NP_005758.2:n.-1346-581_-1346-580delinsAC
NM_000321.3:c.1696-29623_1696-29622delinsGT (RB1) MANE Select NP_000312.2:n.1696-29623_1696-29622delinsGT
NM_001162497.3:c.-1094-581_-1094-580delinsAC (LPAR6) NP_001155969.1:n.-1094-581_-1094-580delinsAC
NM_001377316.2:c.-1094-581_-1094-580delinsAC (LPAR6) NP_001364245.1:n.-1094-581_-1094-580delinsAC
NM_001377317.2:c.-1094-581_-1094-580delinsAC (LPAR6) NP_001364246.1:n.-1094-581_-1094-580delinsAC
NM_005767.7:c.-1346-581_-1346-580delinsAC (LPAR6) NP_005758.2:n.-1346-581_-1346-580delinsAC