Canonical Allele Identifier: CA1293259208

Gene: LRP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963270_140963272delinsCAT , CM000664.2:g.140963270_140963272delinsCAT	GRCh38
NC_000002.11:g.141720839_141720841delinsCAT , CM000664.1:g.141720839_141720841delinsCAT	GRCh37
NC_000002.10:g.141437309_141437311delinsCAT	NCBI36
NG_051023.1:g.1174192_1174194delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11332_2888-11330delinsATG MANE Select	ENSP00000374135.3:n.2888-11332_2888-11330delinsATG
ENST00000389484.7:c.2888-11332_2888-11330delinsATG	ENSP00000374135.3:n.2888-11332_2888-11330delinsATG
ENST00000434794.1:c.323-11332_323-11330delinsATG	ENSP00000413239.1:n.323-11332_323-11330delinsATG
ENST00000618808.4:c.2546-11332_2546-11330delinsATG	ENSP00000478868.1:n.2546-11332_2546-11330delinsATG
NM_018557.2:c.2888-11332_2888-11330delinsATG	NP_061027.2:n.2888-11332_2888-11330delinsATG
XM_011511352.1:c.2999-11332_2999-11330delinsATG	XP_011509654.1:n.2999-11332_2999-11330delinsATG
XM_017004341.1:c.2498-11332_2498-11330delinsATG	XP_016859830.1:n.2498-11332_2498-11330delinsATG
XR_001738778.1:n.4622-11332_4622-11330delinsATG
NM_018557.3:c.2888-11332_2888-11330delinsATG MANE Select	NP_061027.2:n.2888-11332_2888-11330delinsATG