Canonical Allele Identifier: CA2622982711

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48412936del , CM000675.2:g.48412936del GRCh38
NC_000013.10:g.48987072del , CM000675.1:g.48987072del GRCh37
NC_000013.9:g.47885073del NCBI36
NG_009009.1:g.114190del , LRG_517:g.114190del
NG_012874.1:g.36772del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1695+31493del (RB1) MANE Select ENSP00000267163.4:n.1695+31493del
ENST00000620633.5:c.-510del (LPAR6) MANE Select ENSP00000482660.1:n.-510del
ENST00000643064.1:c.194+31493del (RB1)
ENST00000650461.1:c.1695+31493del (RB1) ENSP00000497193.1:n.1695+31493del
ENST00000267163.4:c.1695+31493del (RB1) ENSP00000267163.4:n.1695+31493del
ENST00000345941.2:c.-510del (LPAR6) ENSP00000344353.2:n.-510del
ENST00000378434.8:c.-510del (LPAR6) ENSP00000367691.3:n.-510del
ENST00000462781.5:n.114+2767del (LPAR6)
ENST00000465365.6:n.1068+2767del (LPAR6)
ENST00000470937.1:n.117+2767del (LPAR6)
ENST00000620633.4:c.-510del (LPAR6) ENSP00000482660.1:n.-510del
NM_000321.2:c.1695+31493del , LRG_517t1:c.1695+31493del (RB1) NP_000312.2:n.1695+31493del
NM_001162497.1:c.-510del (LPAR6) NP_001155969.1:n.-510del
NM_001162498.1:c.-510del (LPAR6) NP_001155970.1:n.-510del
NM_005767.5:c.-510del (LPAR6) NP_005758.2:n.-510del
XM_011535171.1:c.1434+31493del (RB1) XP_011533473.1:n.1434+31493del
XM_011535171.2:c.1434+31493del (RB1) XP_011533473.1:n.1434+31493del
XM_024449302.1:c.-510del (LPAR6) XP_024305070.1:n.-510del
XM_024449303.1:c.192+2767del (LPAR6) XP_024305071.1:n.192+2767del
XM_024449304.1:c.192+2767del (LPAR6) XP_024305072.1:n.192+2767del
NM_001162497.2:c.-510del (LPAR6) NP_001155969.1:n.-510del
NM_001162498.2:c.-510del (LPAR6) NP_001155970.1:n.-510del
NM_001377316.1:c.-510del (LPAR6) NP_001364245.1:n.-510del
NM_001377317.1:c.-510del (LPAR6) NP_001364246.1:n.-510del
NM_005767.6:c.-510del (LPAR6) NP_005758.2:n.-510del
NM_000321.3:c.1695+31493del (RB1) MANE Select NP_000312.2:n.1695+31493del
NM_001162497.3:c.-510del (LPAR6) NP_001155969.1:n.-510del
NM_001162498.3:c.-510del (LPAR6) MANE Select NP_001155970.1:n.-510del
NM_001377316.2:c.-510del (LPAR6) NP_001364245.1:n.-510del
NM_001377317.2:c.-510del (LPAR6) NP_001364246.1:n.-510del
NM_005767.7:c.-510del (LPAR6) NP_005758.2:n.-510del