Canonical Allele Identifier: CA56722903

Gene: LRP1B

Linked Data

• dbSNP Id: rs942225331
• gnomAD v2: 2-141720684-G-GC
• gnomAD v3: 2-140963115-G-GC
• gnomAD v4: 2-140963115-G-GC
• MyVariant Identifiers: chr2:g.141720684_141720685insC (hg19) ; chr2:g.140963115_140963116insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963115_140963116insC , CM000664.2:g.140963115_140963116insC	GRCh38
NC_000002.11:g.141720684_141720685insC , CM000664.1:g.141720684_141720685insC	GRCh37
NC_000002.10:g.141437154_141437155insC	NCBI36
NG_051023.1:g.1174348_1174349insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11176_2888-11175insG MANE Select	ENSP00000374135.3:n.2888-11176_2888-11175insG
ENST00000389484.7:c.2888-11176_2888-11175insG	ENSP00000374135.3:n.2888-11176_2888-11175insG
ENST00000434794.1:c.323-11176_323-11175insG	ENSP00000413239.1:n.323-11176_323-11175insG
ENST00000618808.4:c.2546-11176_2546-11175insG	ENSP00000478868.1:n.2546-11176_2546-11175insG
NM_018557.2:c.2888-11176_2888-11175insG	NP_061027.2:n.2888-11176_2888-11175insG
XM_011511352.1:c.2999-11176_2999-11175insG	XP_011509654.1:n.2999-11176_2999-11175insG
XM_017004341.1:c.2498-11176_2498-11175insG	XP_016859830.1:n.2498-11176_2498-11175insG
XR_001738778.1:n.4622-11176_4622-11175insG
NM_018557.3:c.2888-11176_2888-11175insG MANE Select	NP_061027.2:n.2888-11176_2888-11175insG