Canonical Allele Identifier: CA1293259721

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963635_140963636delinsCT , CM000664.2:g.140963635_140963636delinsCT	GRCh38
NC_000002.11:g.141721204_141721205delinsCT , CM000664.1:g.141721204_141721205delinsCT	GRCh37
NC_000002.10:g.141437674_141437675delinsCT	NCBI36
NG_051023.1:g.1173828_1173829delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11696_2888-11695delinsAG MANE Select	ENSP00000374135.3:n.2888-11696_2888-11695delinsAG
ENST00000389484.7:c.2888-11696_2888-11695delinsAG	ENSP00000374135.3:n.2888-11696_2888-11695delinsAG
ENST00000434794.1:c.323-11696_323-11695delinsAG	ENSP00000413239.1:n.323-11696_323-11695delinsAG
ENST00000618808.4:c.2546-11696_2546-11695delinsAG	ENSP00000478868.1:n.2546-11696_2546-11695delinsAG
NM_018557.2:c.2888-11696_2888-11695delinsAG	NP_061027.2:n.2888-11696_2888-11695delinsAG
XM_011511352.1:c.2999-11696_2999-11695delinsAG	XP_011509654.1:n.2999-11696_2999-11695delinsAG
XM_017004341.1:c.2498-11696_2498-11695delinsAG	XP_016859830.1:n.2498-11696_2498-11695delinsAG
XR_001738778.1:n.4622-11696_4622-11695delinsAG
NM_018557.3:c.2888-11696_2888-11695delinsAG MANE Select	NP_061027.2:n.2888-11696_2888-11695delinsAG