Canonical Allele Identifier: CA1293259676
Gene: LRP1B HGNC NCBI

Linked Data

dbSNP Id: rs1696105064

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963598_140963599insTCCAGTT , CM000664.2:g.140963598_140963599insTCCAGTT GRCh38
NC_000002.11:g.141721167_141721168insTCCAGTT , CM000664.1:g.141721167_141721168insTCCAGTT GRCh37
NC_000002.10:g.141437637_141437638insTCCAGTT NCBI36
NG_051023.1:g.1173865_1173866insAACTGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000389484.8:c.2888-11659_2888-11658insAACTGGA MANE Select ENSP00000374135.3:n.2888-11659_2888-11658...
ENST00000389484.7:c.2888-11659_2888-11658insAACTGGA ENSP00000374135.3:n.2888-11659_2888-11658...
ENST00000434794.1:c.323-11659_323-11658insAACTGGA ENSP00000413239.1:n.323-11659_323-11658in...
ENST00000618808.4:c.2546-11659_2546-11658insAACTGGA ENSP00000478868.1:n.2546-11659_2546-11658...
NM_018557.2:c.2888-11659_2888-11658insAACTGGA NP_061027.2:n.2888-11659_2888-11658insAAC...
XM_011511352.1:c.2999-11659_2999-11658insAACTGGA XP_011509654.1:n.2999-11659_2999-11658ins...
XM_017004341.1:c.2498-11659_2498-11658insAACTGGA XP_016859830.1:n.2498-11659_2498-11658ins...
XR_001738778.1:n.4622-11659_4622-11658insAACTGGA
NM_018557.3:c.2888-11659_2888-11658insAACTGGA MANE Select NP_061027.2:n.2888-11659_2888-11658insAAC...