Canonical Allele Identifier: CA2661815129

Gene: LRP2

Linked Data

• gnomAD v4: 2-169154482-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154482_169154483insGG , CM000664.2:g.169154482_169154483insGG	GRCh38
NC_000002.11:g.170010992_170010993insGG , CM000664.1:g.170010992_170010993insGG	GRCh37
NC_000002.10:g.169719238_169719239insGG	NCBI36
NG_012634.1:g.213130_213131insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12272_12273insCC MANE Select	ENSP00000496870.1:p.Trp4091CysfsTer7
ENST00000649153.1:c.3172_3173insCC
ENST00000650252.1:c.1300_1301insCC	ENSP00000496887.1:p.Gly434AlafsTer21
ENST00000263816.7:c.12272_12273insCC	ENSP00000263816.3:p.Trp4091CysfsTer7
NM_004525.2:c.12272_12273insCC	NP_004516.2:p.Trp4091CysfsTer7
XM_011511183.1:c.12143_12144insCC	XP_011509485.1:p.Trp4048CysfsTer7
XM_011511184.1:c.9983_9984insCC	XP_011509486.1:p.Trp3328CysfsTer7
NM_004525.3:c.12272_12273insCC MANE Select	NP_004516.2:p.Trp4091CysfsTer7
XM_011511183.3:c.12143_12144insCC	XP_011509485.1:p.Trp4048CysfsTer7
XM_011511184.2:c.9983_9984insCC	XP_011509486.1:p.Trp3328CysfsTer7