Canonical Allele Identifier: CA1037173491

Gene: LRP1B

Linked Data

• dbSNP Id: rs1696100433
• gnomAD v3: 2-140963460-T-TA
• gnomAD v4: 2-140963460-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963460_140963461insA , CM000664.2:g.140963460_140963461insA	GRCh38
NC_000002.11:g.141721029_141721030insA , CM000664.1:g.141721029_141721030insA	GRCh37
NC_000002.10:g.141437499_141437500insA	NCBI36
NG_051023.1:g.1174003_1174004insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11521_2888-11520insT MANE Select	ENSP00000374135.3:n.2888-11521_2888-11520insT
ENST00000389484.7:c.2888-11521_2888-11520insT	ENSP00000374135.3:n.2888-11521_2888-11520insT
ENST00000434794.1:c.323-11521_323-11520insT	ENSP00000413239.1:n.323-11521_323-11520insT
ENST00000618808.4:c.2546-11521_2546-11520insT	ENSP00000478868.1:n.2546-11521_2546-11520insT
NM_018557.2:c.2888-11521_2888-11520insT	NP_061027.2:n.2888-11521_2888-11520insT
XM_011511352.1:c.2999-11521_2999-11520insT	XP_011509654.1:n.2999-11521_2999-11520insT
XM_017004341.1:c.2498-11521_2498-11520insT	XP_016859830.1:n.2498-11521_2498-11520insT
XR_001738778.1:n.4622-11521_4622-11520insT
NM_018557.3:c.2888-11521_2888-11520insT MANE Select	NP_061027.2:n.2888-11521_2888-11520insT