Canonical Allele Identifier: CA1293294932

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038100A= , CM000664.2:g.141038100A=	GRCh38
NC_000002.11:g.141795669A= , CM000664.1:g.141795669A=	GRCh37
NC_000002.10:g.141512139A=	NCBI36
NG_051023.1:g.1099364T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10886T= MANE Select	ENSP00000374135.3:n.1789+10886T=
ENST00000389484.7:c.1789+10886T=	ENSP00000374135.3:n.1789+10886T=
ENST00000434794.1:c.206-55824T=	ENSP00000413239.1:n.206-55824T=
ENST00000618808.4:c.1447+10886T=	ENSP00000478868.1:n.1447+10886T=
NM_018557.2:c.1789+10886T=	NP_061027.2:n.1789+10886T=
XM_011511352.1:c.1900+10886T=	XP_011509654.1:n.1900+10886T=
XM_017004341.1:c.1399+10886T=	XP_016859830.1:n.1399+10886T=
XR_001738778.1:n.3523+10886T=
NM_018557.3:c.1789+10886T= MANE Select	NP_061027.2:n.1789+10886T=