Canonical Allele Identifier: CA2089994754

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48411870_48411875delinsACAATC , CM000675.2:g.48411870_48411875delinsACAATC GRCh38
NC_000013.10:g.48986006_48986011delinsACAATC , CM000675.1:g.48986006_48986011delinsACAATC GRCh37
NC_000013.9:g.47884007_47884012delinsACAATC NCBI36
NG_009009.1:g.113124_113129delinsACAATC , LRG_517:g.113124_113129delinsACAATC
NG_012874.1:g.37830_37835delinsGATTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1695+30427_1695+30432delinsACAATC (RB1) MANE Select ENSP00000267163.4:n.1695+30427_1695+30432...
ENST00000620633.5:c.549_554delinsGATTGT (LPAR6) MANE Select ENSP00000482660.1:p.Arg183=
ENST00000643064.1:c.194+30427_194+30432delinsACAATC (RB1)
ENST00000650461.1:c.1695+30427_1695+30432delinsACAATC (RB1) ENSP00000497193.1:n.1695+30427_1695+30432...
ENST00000267163.4:c.1695+30427_1695+30432delinsACAATC (RB1) ENSP00000267163.4:n.1695+30427_1695+30432...
ENST00000345941.2:c.549_554delinsGATTGT (LPAR6) ENSP00000344353.2:p.Arg183=
ENST00000378434.8:c.549_554delinsGATTGT (LPAR6) ENSP00000367691.3:p.Arg183=
ENST00000462781.5:n.114+3825_114+3830delinsGATTGT (LPAR6)
ENST00000465365.6:n.1069-3108_1069-3103delinsGATTGT (LPAR6)
ENST00000470937.1:n.117+3825_117+3830delinsGATTGT (LPAR6)
ENST00000482024.1:n.400_405delinsGATTGT (LPAR6)
ENST00000620633.4:c.549_554delinsGATTGT (LPAR6) ENSP00000482660.1:p.Arg183=
NM_000321.2:c.1695+30427_1695+30432delinsACAATC , LRG_517t1:c.1695+30427_1695+30432delinsACAATC (RB1) NP_000312.2:n.1695+30427_1695+30432delins...
NM_001162497.1:c.549_554delinsGATTGT (LPAR6) NP_001155969.1:p.Arg183=
NM_001162498.1:c.549_554delinsGATTGT (LPAR6) NP_001155970.1:p.Arg183=
NM_005767.5:c.549_554delinsGATTGT (LPAR6) NP_005758.2:p.Arg183=
XM_011535171.1:c.1434+30427_1434+30432delinsACAATC (RB1) XP_011533473.1:n.1434+30427_1434+30432del...
XM_011535171.2:c.1434+30427_1434+30432delinsACAATC (RB1) XP_011533473.1:n.1434+30427_1434+30432del...
XM_024449302.1:c.549_554delinsGATTGT (LPAR6) XP_024305070.1:p.Arg183=
XM_024449303.1:c.192+3825_192+3830delinsGATTGT (LPAR6) XP_024305071.1:n.192+3825_192+3830delinsG...
XM_024449304.1:c.192+3825_192+3830delinsGATTGT (LPAR6) XP_024305072.1:n.192+3825_192+3830delinsG...
NM_001162497.2:c.549_554delinsGATTGT (LPAR6) NP_001155969.1:p.Arg183=
NM_001162498.2:c.549_554delinsGATTGT (LPAR6) NP_001155970.1:p.Arg183=
NM_001377316.1:c.549_554delinsGATTGT (LPAR6) NP_001364245.1:p.Arg183=
NM_001377317.1:c.549_554delinsGATTGT (LPAR6) NP_001364246.1:p.Arg183=
NM_005767.6:c.549_554delinsGATTGT (LPAR6) NP_005758.2:p.Arg183=
NM_000321.3:c.1695+30427_1695+30432delinsACAATC (RB1) MANE Select NP_000312.2:n.1695+30427_1695+30432delins...
NM_001162497.3:c.549_554delinsGATTGT (LPAR6) NP_001155969.1:p.Arg183=
NM_001162498.3:c.549_554delinsGATTGT (LPAR6) MANE Select NP_001155970.1:p.Arg183=
NM_001377316.2:c.549_554delinsGATTGT (LPAR6) NP_001364245.1:p.Arg183=
NM_001377317.2:c.549_554delinsGATTGT (LPAR6) NP_001364246.1:p.Arg183=
NM_005767.7:c.549_554delinsGATTGT (LPAR6) NP_005758.2:p.Arg183=