Canonical Allele Identifier: CA237753959
Gene: LRP1 HGNC NCBI

Linked Data

dbSNP Id: rs1018775331
MyVariant Identifiers: chr12:g.57534561G>A (hg19) chr12:g.57140778G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57140778G>A , CM000674.2:g.57140778G>A GRCh38
NC_000012.11:g.57534561G>A , CM000674.1:g.57534561G>A GRCh37
NC_000012.10:g.55820828G>A NCBI36
NG_016444.1:g.17280G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243077.8:c.191-596G>A MANE Select ENSP00000243077.3:n.191-596G>A
ENST00000243077.7:c.191-596G>A ENSP00000243077.3:n.191-596G>A
ENST00000338962.8:c.191-596G>A ENSP00000341264.4:n.191-596G>A
ENST00000553277.5:c.191-596G>A ENSP00000451449.1:n.191-596G>A
ENST00000554174.1:c.191-596G>A ENSP00000451737.1:n.191-596G>A
NM_002332.2:c.191-596G>A NP_002323.2:n.191-596G>A
XM_017019303.1:c.191-596G>A XP_016874792.1:n.191-596G>A
NM_002332.3:c.191-596G>A MANE Select NP_002323.2:n.191-596G>A
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