Canonical Allele Identifier: CA2605191566

Gene: LRP1B

Linked Data

• gnomAD v3: 2-140963111-TTC-T
• gnomAD v4: 2-140963111-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963113_140963114del , CM000664.2:g.140963113_140963114del	GRCh38
NC_000002.11:g.141720682_141720683del , CM000664.1:g.141720682_141720683del	GRCh37
NC_000002.10:g.141437152_141437153del	NCBI36
NG_051023.1:g.1174351_1174352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11173_2888-11172del MANE Select	ENSP00000374135.3:n.2888-11173_2888-11172del
ENST00000389484.7:c.2888-11173_2888-11172del	ENSP00000374135.3:n.2888-11173_2888-11172del
ENST00000434794.1:c.323-11173_323-11172del	ENSP00000413239.1:n.323-11173_323-11172del
ENST00000618808.4:c.2546-11173_2546-11172del	ENSP00000478868.1:n.2546-11173_2546-11172del
NM_018557.2:c.2888-11173_2888-11172del	NP_061027.2:n.2888-11173_2888-11172del
XM_011511352.1:c.2999-11173_2999-11172del	XP_011509654.1:n.2999-11173_2999-11172del
XM_017004341.1:c.2498-11173_2498-11172del	XP_016859830.1:n.2498-11173_2498-11172del
XR_001738778.1:n.4622-11173_4622-11172del
NM_018557.3:c.2888-11173_2888-11172del MANE Select	NP_061027.2:n.2888-11173_2888-11172del