Canonical Allele Identifier: CA1293501230

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141470940C= , CM000664.2:g.141470940C=	GRCh38
NC_000002.11:g.142228509C= , CM000664.1:g.142228509C=	GRCh37
NC_000002.10:g.141944979C=	NCBI36
NG_051023.1:g.666524G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.343+9456G= MANE Select	ENSP00000374135.3:n.343+9456G=
ENST00000389484.7:c.343+9456G=	ENSP00000374135.3:n.343+9456G=
ENST00000434794.1:c.205+339339G=	ENSP00000413239.1:n.205+339339G=
NM_018557.2:c.343+9456G=	NP_061027.2:n.343+9456G=
XM_011511352.1:c.454+9456G=	XP_011509654.1:n.454+9456G=
XR_923384.1:n.1693C=
XR_923385.1:n.1793C=
XR_923386.1:n.624-97C=
XM_017004341.1:c.-48+9456G=	XP_016859830.1:n.-48+9456G=
XR_001738778.1:n.2077+9456G=
NM_018557.3:c.343+9456G= MANE Select	NP_061027.2:n.343+9456G=