Canonical Allele Identifier: CA2038728980
Gene: LRP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57139122C= , CM000674.2:g.57139122C= GRCh38
NC_000012.11:g.57532905C= , CM000674.1:g.57532905C= GRCh37
NC_000012.10:g.55819172C= NCBI36
NG_016444.1:g.15624C=

Transcript Alleles

HGVS Amino-acid change
ENST00000243077.8:c.190+541C= MANE Select ENSP00000243077.3:n.190+541C=
ENST00000243077.7:c.190+541C= ENSP00000243077.3:n.190+541C=
ENST00000338962.8:c.190+541C= ENSP00000341264.4:n.190+541C=
ENST00000553277.5:c.190+541C= ENSP00000451449.1:n.190+541C=
ENST00000554174.1:c.190+541C= ENSP00000451737.1:n.190+541C=
NM_002332.2:c.190+541C= NP_002323.2:n.190+541C=
XM_017019303.1:c.190+541C= XP_016874792.1:n.190+541C=
NM_002332.3:c.190+541C= MANE Select NP_002323.2:n.190+541C=
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