Canonical Allele Identifier: CA2038730169
Gene: LRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57140755A= , CM000674.2:g.57140755A= GRCh38
NC_000012.11:g.57534538A= , CM000674.1:g.57534538A= GRCh37
NC_000012.10:g.55820805A= NCBI36
NG_016444.1:g.17257A=

Transcript Alleles

HGVS Amino-acid change
ENST00000243077.8:c.191-619A= MANE Select ENSP00000243077.3:n.191-619A=
ENST00000243077.7:c.191-619A= ENSP00000243077.3:n.191-619A=
ENST00000338962.8:c.191-619A= ENSP00000341264.4:n.191-619A=
ENST00000553277.5:c.191-619A= ENSP00000451449.1:n.191-619A=
ENST00000554174.1:c.191-619A= ENSP00000451737.1:n.191-619A=
NM_002332.2:c.191-619A= NP_002323.2:n.191-619A=
XM_017019303.1:c.191-619A= XP_016874792.1:n.191-619A=
NM_002332.3:c.191-619A= MANE Select NP_002323.2:n.191-619A=