Canonical Allele Identifier: CA388158825

Gene: RB1 LPAR6

Linked Data

• MyVariant Identifiers: chr13:g.48985964A>G (hg19) ; chr13:g.48411828A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48411828A>G , CM000675.2:g.48411828A>G	GRCh38
NC_000013.10:g.48985964A>G , CM000675.1:g.48985964A>G	GRCh37
NC_000013.9:g.47883965A>G	NCBI36
NG_009009.1:g.113082A>G , LRG_517:g.113082A>G
NG_012874.1:g.37877T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1695+30385A>G (RB1) MANE Select	ENSP00000267163.4:n.1695+30385A>G
ENST00000620633.5:c.596T>C (LPAR6) MANE Select	ENSP00000482660.1:p.Leu199Ser
ENST00000643064.1:c.194+30385A>G (RB1)
ENST00000650461.1:c.1695+30385A>G (RB1)	ENSP00000497193.1:n.1695+30385A>G
ENST00000267163.4:c.1695+30385A>G (RB1)	ENSP00000267163.4:n.1695+30385A>G
ENST00000345941.2:c.596T>C (LPAR6)	ENSP00000344353.2:p.Leu199Ser
ENST00000378434.8:c.596T>C (LPAR6)	ENSP00000367691.3:p.Leu199Ser
ENST00000462781.5:n.114+3872T>C (LPAR6)
ENST00000465365.6:n.1069-3061T>C (LPAR6)
ENST00000470937.1:n.117+3872T>C (LPAR6)
ENST00000482024.1:n.447T>C (LPAR6)
ENST00000620633.4:c.596T>C (LPAR6)	ENSP00000482660.1:p.Leu199Ser
NM_000321.2:c.1695+30385A>G , LRG_517t1:c.1695+30385A>G (RB1)	NP_000312.2:n.1695+30385A>G
NM_001162497.1:c.596T>C (LPAR6)	NP_001155969.1:p.Leu199Ser
NM_001162498.1:c.596T>C (LPAR6)	NP_001155970.1:p.Leu199Ser
NM_005767.5:c.596T>C (LPAR6)	NP_005758.2:p.Leu199Ser
XM_011535171.1:c.1434+30385A>G (RB1)	XP_011533473.1:n.1434+30385A>G
XM_011535171.2:c.1434+30385A>G (RB1)	XP_011533473.1:n.1434+30385A>G
XM_024449302.1:c.596T>C (LPAR6)	XP_024305070.1:p.Leu199Ser
XM_024449303.1:c.192+3872T>C (LPAR6)	XP_024305071.1:n.192+3872T>C
XM_024449304.1:c.192+3872T>C (LPAR6)	XP_024305072.1:n.192+3872T>C
NM_001162497.2:c.596T>C (LPAR6)	NP_001155969.1:p.Leu199Ser
NM_001162498.2:c.596T>C (LPAR6)	NP_001155970.1:p.Leu199Ser
NM_001377316.1:c.596T>C (LPAR6)	NP_001364245.1:p.Leu199Ser
NM_001377317.1:c.596T>C (LPAR6)	NP_001364246.1:p.Leu199Ser
NM_005767.6:c.596T>C (LPAR6)	NP_005758.2:p.Leu199Ser
NM_000321.3:c.1695+30385A>G (RB1) MANE Select	NP_000312.2:n.1695+30385A>G
NM_001162497.3:c.596T>C (LPAR6)	NP_001155969.1:p.Leu199Ser
NM_001162498.3:c.596T>C (LPAR6) MANE Select	NP_001155970.1:p.Leu199Ser
NM_001377316.2:c.596T>C (LPAR6)	NP_001364245.1:p.Leu199Ser
NM_001377317.2:c.596T>C (LPAR6)	NP_001364246.1:p.Leu199Ser
NM_005767.7:c.596T>C (LPAR6)	NP_005758.2:p.Leu199Ser