Canonical Allele Identifier: CA2661815130

Gene: LRP2

Linked Data

• gnomAD v4: 2-169154483-C-CAATCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154489_169154494dup , CM000664.2:g.169154489_169154494dup	GRCh38
NC_000002.11:g.170010999_170011004dup , CM000664.1:g.170010999_170011004dup	GRCh37
NC_000002.10:g.169719245_169719250dup	NCBI36
NG_012634.1:g.213124_213129dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12266_12271dup MANE Select	ENSP00000496870.1:p.Asp4090_Trp4091insTyr...
ENST00000649153.1:c.3166_3171dup
ENST00000650252.1:c.1294_1299dup	ENSP00000496887.1:p.Ile433_Gly434insMetIl...
ENST00000263816.7:c.12266_12271dup	ENSP00000263816.3:p.Asp4090_Trp4091insTyr...
NM_004525.2:c.12266_12271dup	NP_004516.2:p.Asp4090_Trp4091insTyrAsp
XM_011511183.1:c.12137_12142dup	XP_011509485.1:p.Asp4047_Trp4048insTyrAsp...
XM_011511184.1:c.9977_9982dup	XP_011509486.1:p.Asp3327_Trp3328insTyrAsp...
NM_004525.3:c.12266_12271dup MANE Select	NP_004516.2:p.Asp4090_Trp4091insTyrAsp
XM_011511183.3:c.12137_12142dup	XP_011509485.1:p.Asp4047_Trp4048insTyrAsp...
XM_011511184.2:c.9977_9982dup	XP_011509486.1:p.Asp3327_Trp3328insTyrAsp...