Canonical Allele Identifier: CA2038723882
Gene: LRP1 HGNC NCBI

Linked Data

dbSNP Id: rs2035078831
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57133358A>G , CM000674.2:g.57133358A>G GRCh38
NC_000012.11:g.57527141A>G , CM000674.1:g.57527141A>G GRCh37
NC_000012.10:g.55813408A>G NCBI36
NG_016444.1:g.9860A>G
NG_021272.2:g.3782T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243077.8:c.67+4327A>G MANE Select ENSP00000243077.3:n.67+4327A>G
ENST00000243077.7:c.67+4327A>G ENSP00000243077.3:n.67+4327A>G
ENST00000338962.8:c.67+4327A>G ENSP00000341264.4:n.67+4327A>G
ENST00000553277.5:c.67+4327A>G ENSP00000451449.1:n.67+4327A>G
ENST00000554174.1:c.67+4327A>G ENSP00000451737.1:n.67+4327A>G
NM_002332.2:c.67+4327A>G NP_002323.2:n.67+4327A>G
XM_017019303.1:c.67+4327A>G XP_016874792.1:n.67+4327A>G
NM_002332.3:c.67+4327A>G MANE Select NP_002323.2:n.67+4327A>G
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