Canonical Allele Identifier: CA536106276

Gene: LRP1B

Linked Data

• dbSNP Id: rs140209072
• gnomAD v2: 2-141721012-TTATATA-T
• gnomAD v3: 2-140963443-TTATATA-T
• gnomAD v4: 2-140963443-TTATATA-T
• MyVariant Identifiers: chr2:g.141721015_141721020del (hg19) ; chr2:g.141721013_141721018del (hg19) ; chr2:g.140963446_140963451del (hg38) ; chr2:g.140963444_140963449del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.140963455_140963460del , CM000664.2:g.140963455_140963460del	GRCh38
NC_000002.11:g.141721024_141721029del , CM000664.1:g.141721024_141721029del	GRCh37
NC_000002.10:g.141437494_141437499del	NCBI36
NG_051023.1:g.1174015_1174020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389484.8:c.2888-11509_2888-11504del MANE Select	ENSP00000374135.3:n.2888-11509_2888-11504del
ENST00000389484.7:c.2888-11509_2888-11504del	ENSP00000374135.3:n.2888-11509_2888-11504del
ENST00000434794.1:c.323-11509_323-11504del	ENSP00000413239.1:n.323-11509_323-11504del
ENST00000618808.4:c.2546-11509_2546-11504del	ENSP00000478868.1:n.2546-11509_2546-11504del
NM_018557.2:c.2888-11509_2888-11504del	NP_061027.2:n.2888-11509_2888-11504del
XM_011511352.1:c.2999-11509_2999-11504del	XP_011509654.1:n.2999-11509_2999-11504del
XM_017004341.1:c.2498-11509_2498-11504del	XP_016859830.1:n.2498-11509_2498-11504del
XR_001738778.1:n.4622-11509_4622-11504del
NM_018557.3:c.2888-11509_2888-11504del MANE Select	NP_061027.2:n.2888-11509_2888-11504del