Canonical Allele Identifier: CA948066592
Gene: LRP1 HGNC NCBI

Linked Data

dbSNP Id: rs2035077559

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57133314C>T , CM000674.2:g.57133314C>T GRCh38
NC_000012.11:g.57527097C>T , CM000674.1:g.57527097C>T GRCh37
NC_000012.10:g.55813364C>T NCBI36
NG_016444.1:g.9816C>T
NG_021272.2:g.3826G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243077.8:c.67+4283C>T MANE Select ENSP00000243077.3:n.67+4283C>T
ENST00000243077.7:c.67+4283C>T ENSP00000243077.3:n.67+4283C>T
ENST00000338962.8:c.67+4283C>T ENSP00000341264.4:n.67+4283C>T
ENST00000553277.5:c.67+4283C>T ENSP00000451449.1:n.67+4283C>T
ENST00000554174.1:c.67+4283C>T ENSP00000451737.1:n.67+4283C>T
NM_002332.2:c.67+4283C>T NP_002323.2:n.67+4283C>T
XM_017019303.1:c.67+4283C>T XP_016874792.1:n.67+4283C>T
NM_002332.3:c.67+4283C>T MANE Select NP_002323.2:n.67+4283C>T