Canonical Allele Identifier: CA2089995020

Gene: RB1 LPAR6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48412511_48412512delinsCA , CM000675.2:g.48412511_48412512delinsCA	GRCh38
NC_000013.10:g.48986647_48986648delinsCA , CM000675.1:g.48986647_48986648delinsCA	GRCh37
NC_000013.9:g.47884648_47884649delinsCA	NCBI36
NG_009009.1:g.113765_113766delinsCA , LRG_517:g.113765_113766delinsCA
NG_012874.1:g.37193_37194delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1695+31068_1695+31069delinsCA (RB1) MANE Select	ENSP00000267163.4:n.1695+31068_1695+31069delinsCA
ENST00000620633.5:c.-89_-88delinsTG (LPAR6) MANE Select	ENSP00000482660.1:n.-89_-88delinsTG
ENST00000643064.1:c.194+31068_194+31069delinsCA (RB1)
ENST00000650461.1:c.1695+31068_1695+31069delinsCA (RB1)	ENSP00000497193.1:n.1695+31068_1695+31069delinsCA
ENST00000267163.4:c.1695+31068_1695+31069delinsCA (RB1)	ENSP00000267163.4:n.1695+31068_1695+31069delinsCA
ENST00000345941.2:c.-89_-88delinsTG (LPAR6)	ENSP00000344353.2:n.-89_-88delinsTG
ENST00000378434.8:c.-89_-88delinsTG (LPAR6)	ENSP00000367691.3:n.-89_-88delinsTG
ENST00000462781.5:n.114+3188_114+3189delinsTG (LPAR6)
ENST00000465365.6:n.1068+3188_1068+3189delinsTG (LPAR6)
ENST00000470937.1:n.117+3188_117+3189delinsTG (LPAR6)
ENST00000620633.4:c.-89_-88delinsTG (LPAR6)	ENSP00000482660.1:n.-89_-88delinsTG
NM_000321.2:c.1695+31068_1695+31069delinsCA , LRG_517t1:c.1695+31068_1695+31069delinsCA (RB1)	NP_000312.2:n.1695+31068_1695+31069delinsCA
NM_001162497.1:c.-89_-88delinsTG (LPAR6)	NP_001155969.1:n.-89_-88delinsTG
NM_001162498.1:c.-89_-88delinsTG (LPAR6)	NP_001155970.1:n.-89_-88delinsTG
NM_005767.5:c.-89_-88delinsTG (LPAR6)	NP_005758.2:n.-89_-88delinsTG
XM_011535171.1:c.1434+31068_1434+31069delinsCA (RB1)	XP_011533473.1:n.1434+31068_1434+31069delinsCA
XM_011535171.2:c.1434+31068_1434+31069delinsCA (RB1)	XP_011533473.1:n.1434+31068_1434+31069delinsCA
XM_024449302.1:c.-89_-88delinsTG (LPAR6)	XP_024305070.1:n.-89_-88delinsTG
XM_024449303.1:c.192+3188_192+3189delinsTG (LPAR6)	XP_024305071.1:n.192+3188_192+3189delinsTG
XM_024449304.1:c.192+3188_192+3189delinsTG (LPAR6)	XP_024305072.1:n.192+3188_192+3189delinsTG
NM_001162497.2:c.-89_-88delinsTG (LPAR6)	NP_001155969.1:n.-89_-88delinsTG
NM_001162498.2:c.-89_-88delinsTG (LPAR6)	NP_001155970.1:n.-89_-88delinsTG
NM_001377316.1:c.-89_-88delinsTG (LPAR6)	NP_001364245.1:n.-89_-88delinsTG
NM_001377317.1:c.-89_-88delinsTG (LPAR6)	NP_001364246.1:n.-89_-88delinsTG
NM_005767.6:c.-89_-88delinsTG (LPAR6)	NP_005758.2:n.-89_-88delinsTG
NM_000321.3:c.1695+31068_1695+31069delinsCA (RB1) MANE Select	NP_000312.2:n.1695+31068_1695+31069delinsCA
NM_001162497.3:c.-89_-88delinsTG (LPAR6)	NP_001155969.1:n.-89_-88delinsTG
NM_001162498.3:c.-89_-88delinsTG (LPAR6) MANE Select	NP_001155970.1:n.-89_-88delinsTG
NM_001377316.2:c.-89_-88delinsTG (LPAR6)	NP_001364245.1:n.-89_-88delinsTG
NM_001377317.2:c.-89_-88delinsTG (LPAR6)	NP_001364246.1:n.-89_-88delinsTG
NM_005767.7:c.-89_-88delinsTG (LPAR6)	NP_005758.2:n.-89_-88delinsTG