Canonical Allele Identifier: CA2038728999
Gene: LRP1 HGNC NCBI

Linked Data

dbSNP Id: rs2035235248
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57139149T>C , CM000674.2:g.57139149T>C GRCh38
NC_000012.11:g.57532932T>C , CM000674.1:g.57532932T>C GRCh37
NC_000012.10:g.55819199T>C NCBI36
NG_016444.1:g.15651T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000243077.8:c.190+568T>C MANE Select ENSP00000243077.3:n.190+568T>C
ENST00000243077.7:c.190+568T>C ENSP00000243077.3:n.190+568T>C
ENST00000338962.8:c.190+568T>C ENSP00000341264.4:n.190+568T>C
ENST00000553277.5:c.190+568T>C ENSP00000451449.1:n.190+568T>C
ENST00000554174.1:c.190+568T>C ENSP00000451737.1:n.190+568T>C
NM_002332.2:c.190+568T>C NP_002323.2:n.190+568T>C
XM_017019303.1:c.190+568T>C XP_016874792.1:n.190+568T>C
NM_002332.3:c.190+568T>C MANE Select NP_002323.2:n.190+568T>C
Search 100 bp 5'
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