Canonical Allele Identifier: CA2544264771

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48412940_48412941insATTTGT , CM000675.2:g.48412940_48412941insATTTGT GRCh38
NC_000013.10:g.48987076_48987077insATTTGT , CM000675.1:g.48987076_48987077insATTTGT GRCh37
NC_000013.9:g.47885077_47885078insATTTGT NCBI36
NG_009009.1:g.114194_114195insATTTGT , LRG_517:g.114194_114195insATTTGT
NG_012874.1:g.36765_36766insCAAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1695+31497_1695+31498insATTTGT (RB1) MANE Select ENSP00000267163.4:n.1695+31497_1695+31498insATTTGT
ENST00000620633.5:c.-517_-516insCAAATA (LPAR6) MANE Select ENSP00000482660.1:n.-517_-516insCAAATA
ENST00000643064.1:c.194+31497_194+31498insATTTGT (RB1)
ENST00000650461.1:c.1695+31497_1695+31498insATTTGT (RB1) ENSP00000497193.1:n.1695+31497_1695+31498insATTTGT
ENST00000267163.4:c.1695+31497_1695+31498insATTTGT (RB1) ENSP00000267163.4:n.1695+31497_1695+31498insATTTGT
ENST00000345941.2:c.-517_-516insCAAATA (LPAR6) ENSP00000344353.2:n.-517_-516insCAAATA
ENST00000378434.8:c.-517_-516insCAAATA (LPAR6) ENSP00000367691.3:n.-517_-516insCAAATA
ENST00000462781.5:n.114+2760_114+2761insCAAATA (LPAR6)
ENST00000465365.6:n.1068+2760_1068+2761insCAAATA (LPAR6)
ENST00000470937.1:n.117+2760_117+2761insCAAATA (LPAR6)
ENST00000620633.4:c.-517_-516insCAAATA (LPAR6) ENSP00000482660.1:n.-517_-516insCAAATA
NM_000321.2:c.1695+31497_1695+31498insATTTGT , LRG_517t1:c.1695+31497_1695+31498insATTTGT (RB1) NP_000312.2:n.1695+31497_1695+31498insATTTGT
NM_001162497.1:c.-517_-516insCAAATA (LPAR6) NP_001155969.1:n.-517_-516insCAAATA
NM_001162498.1:c.-517_-516insCAAATA (LPAR6) NP_001155970.1:n.-517_-516insCAAATA
NM_005767.5:c.-517_-516insCAAATA (LPAR6) NP_005758.2:n.-517_-516insCAAATA
XM_011535171.1:c.1434+31497_1434+31498insATTTGT (RB1) XP_011533473.1:n.1434+31497_1434+31498insATTTGT
XM_011535171.2:c.1434+31497_1434+31498insATTTGT (RB1) XP_011533473.1:n.1434+31497_1434+31498insATTTGT
XM_024449302.1:c.-517_-516insCAAATA (LPAR6) XP_024305070.1:n.-517_-516insCAAATA
XM_024449303.1:c.192+2760_192+2761insCAAATA (LPAR6) XP_024305071.1:n.192+2760_192+2761insCAAATA
XM_024449304.1:c.192+2760_192+2761insCAAATA (LPAR6) XP_024305072.1:n.192+2760_192+2761insCAAATA
NM_001162497.2:c.-517_-516insCAAATA (LPAR6) NP_001155969.1:n.-517_-516insCAAATA
NM_001162498.2:c.-517_-516insCAAATA (LPAR6) NP_001155970.1:n.-517_-516insCAAATA
NM_001377316.1:c.-517_-516insCAAATA (LPAR6) NP_001364245.1:n.-517_-516insCAAATA
NM_001377317.1:c.-517_-516insCAAATA (LPAR6) NP_001364246.1:n.-517_-516insCAAATA
NM_005767.6:c.-517_-516insCAAATA (LPAR6) NP_005758.2:n.-517_-516insCAAATA
NM_000321.3:c.1695+31497_1695+31498insATTTGT (RB1) MANE Select NP_000312.2:n.1695+31497_1695+31498insATTTGT
NM_001162497.3:c.-517_-516insCAAATA (LPAR6) NP_001155969.1:n.-517_-516insCAAATA
NM_001162498.3:c.-517_-516insCAAATA (LPAR6) MANE Select NP_001155970.1:n.-517_-516insCAAATA
NM_001377316.2:c.-517_-516insCAAATA (LPAR6) NP_001364245.1:n.-517_-516insCAAATA
NM_001377317.2:c.-517_-516insCAAATA (LPAR6) NP_001364246.1:n.-517_-516insCAAATA
NM_005767.7:c.-517_-516insCAAATA (LPAR6) NP_005758.2:n.-517_-516insCAAATA