Canonical Allele Identifier: CA2038723872
Gene: LRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57133333G= , CM000674.2:g.57133333G= GRCh38
NC_000012.11:g.57527116G= , CM000674.1:g.57527116G= GRCh37
NC_000012.10:g.55813383G= NCBI36
NG_016444.1:g.9835G=
NG_021272.2:g.3807C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243077.8:c.67+4302G= MANE Select ENSP00000243077.3:n.67+4302G=
ENST00000243077.7:c.67+4302G= ENSP00000243077.3:n.67+4302G=
ENST00000338962.8:c.67+4302G= ENSP00000341264.4:n.67+4302G=
ENST00000553277.5:c.67+4302G= ENSP00000451449.1:n.67+4302G=
ENST00000554174.1:c.67+4302G= ENSP00000451737.1:n.67+4302G=
NM_002332.2:c.67+4302G= NP_002323.2:n.67+4302G=
XM_017019303.1:c.67+4302G= XP_016874792.1:n.67+4302G=
NM_002332.3:c.67+4302G= MANE Select NP_002323.2:n.67+4302G=