Canonical Allele Identifier: CA2700934542

Gene: LRP2

Linked Data

• dbSNP Id: rs2105394632

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247351_169247352insG , CM000664.2:g.169247351_169247352insG	GRCh38
NC_000002.11:g.170103861_170103862insG , CM000664.1:g.170103861_170103862insG	GRCh37
NC_000002.10:g.169812107_169812108insG	NCBI36
NG_012634.1:g.120261_120262insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.2908+26_2908+27insC MANE Select	ENSP00000496870.1:n.2908+26_2908+27insC
ENST00000263816.7:c.2908+26_2908+27insC	ENSP00000263816.3:n.2908+26_2908+27insC
ENST00000443831.1:c.2497+26_2497+27insC	ENSP00000409813.1:n.2497+26_2497+27insC
NM_004525.2:c.2908+26_2908+27insC	NP_004516.2:n.2908+26_2908+27insC
XM_011511183.1:c.2908+26_2908+27insC	XP_011509485.1:n.2908+26_2908+27insC
XM_011511184.1:c.619+26_619+27insC	XP_011509486.1:n.619+26_619+27insC
XM_011511185.1:c.2908+26_2908+27insC	XP_011509487.1:n.2908+26_2908+27insC
NM_004525.3:c.2908+26_2908+27insC MANE Select	NP_004516.2:n.2908+26_2908+27insC
XM_011511183.3:c.2908+26_2908+27insC	XP_011509485.1:n.2908+26_2908+27insC
XM_011511184.2:c.619+26_619+27insC	XP_011509486.1:n.619+26_619+27insC