Canonical Allele Identifier: CA2089999783

Gene: RB1 LPAR6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48423397C= , CM000675.2:g.48423397C=	GRCh38
NC_000013.10:g.48997533C= , CM000675.1:g.48997533C=	GRCh37
NC_000013.9:g.47895534C=	NCBI36
NG_009009.1:g.124651C= , LRG_517:g.124651C=
NG_012874.1:g.26308G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1696-29596C= (RB1) MANE Select	ENSP00000267163.4:n.1696-29596C=
ENST00000643064.1:c.194+41954C= (RB1)
ENST00000650461.1:c.1696-29596C= (RB1)	ENSP00000497193.1:n.1696-29596C=
ENST00000267163.4:c.1696-29596C= (RB1)	ENSP00000267163.4:n.1696-29596C=
ENST00000345941.2:c.-1094-607G= (LPAR6)	ENSP00000344353.2:n.-1094-607G=
ENST00000378434.8:c.-1347+596G= (LPAR6)	ENSP00000367691.3:n.-1347+596G=
ENST00000465365.6:n.662+596G= (LPAR6)
NM_000321.2:c.1696-29596C= , LRG_517t1:c.1696-29596C= (RB1)	NP_000312.2:n.1696-29596C=
NM_001162497.1:c.-1094-607G= (LPAR6)	NP_001155969.1:n.-1094-607G=
NM_005767.5:c.-1347+596G= (LPAR6)	NP_005758.2:n.-1347+596G=
XM_011535171.1:c.1435-29596C= (RB1)	XP_011533473.1:n.1435-29596C=
XM_011535171.2:c.1435-29596C= (RB1)	XP_011533473.1:n.1435-29596C=
NM_001162497.2:c.-1094-607G= (LPAR6)	NP_001155969.1:n.-1094-607G=
NM_001377316.1:c.-1094-607G= (LPAR6)	NP_001364245.1:n.-1094-607G=
NM_001377317.1:c.-1094-607G= (LPAR6)	NP_001364246.1:n.-1094-607G=
NM_005767.6:c.-1347+596G= (LPAR6)	NP_005758.2:n.-1347+596G=
NM_000321.3:c.1696-29596C= (RB1) MANE Select	NP_000312.2:n.1696-29596C=
NM_001162497.3:c.-1094-607G= (LPAR6)	NP_001155969.1:n.-1094-607G=
NM_001377316.2:c.-1094-607G= (LPAR6)	NP_001364245.1:n.-1094-607G=
NM_001377317.2:c.-1094-607G= (LPAR6)	NP_001364246.1:n.-1094-607G=
NM_005767.7:c.-1347+596G= (LPAR6)	NP_005758.2:n.-1347+596G=