Canonical Allele Identifier: CA948066621

Gene: LRP1

Linked Data

• dbSNP Id: rs2035080871
• gnomAD v3: 12-57133456-C-CTTTTG
• gnomAD v4: 12-57133456-C-CTTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57133457_57133458insTTTGT , CM000674.2:g.57133457_57133458insTTTGT	GRCh38
NC_000012.11:g.57527240_57527241insTTTGT , CM000674.1:g.57527240_57527241insTTTGT	GRCh37
NC_000012.10:g.55813507_55813508insTTTGT	NCBI36
NG_016444.1:g.9959_9960insTTTGT
NG_021272.2:g.3683_3684insCAAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000243077.8:c.67+4426_67+4427insTTTGT MANE Select	ENSP00000243077.3:n.67+4426_67+4427insTTT...
ENST00000243077.7:c.67+4426_67+4427insTTTGT	ENSP00000243077.3:n.67+4426_67+4427insTTT...
ENST00000338962.8:c.67+4426_67+4427insTTTGT	ENSP00000341264.4:n.67+4426_67+4427insTTT...
ENST00000553277.5:c.67+4426_67+4427insTTTGT	ENSP00000451449.1:n.67+4426_67+4427insTTT...
ENST00000554174.1:c.67+4426_67+4427insTTTGT	ENSP00000451737.1:n.67+4426_67+4427insTTT...
NM_002332.2:c.67+4426_67+4427insTTTGT	NP_002323.2:n.67+4426_67+4427insTTTGT
XM_017019303.1:c.67+4426_67+4427insTTTGT	XP_016874792.1:n.67+4426_67+4427insTTTGT
NM_002332.3:c.67+4426_67+4427insTTTGT MANE Select	NP_002323.2:n.67+4426_67+4427insTTTGT