Canonical Allele Identifier: CA1306349776

Gene: LRP2

Linked Data

• dbSNP Id: rs1690064737

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247668_169247670del , CM000664.2:g.169247668_169247670del	GRCh38
NC_000002.11:g.170104178_170104180del , CM000664.1:g.170104178_170104180del	GRCh37
NC_000002.10:g.169812424_169812426del	NCBI36
NG_012634.1:g.119945_119947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2771-153_2771-151del MANE Select	ENSP00000496870.1:n.2771-153_2771-151del
ENST00000263816.7:c.2771-153_2771-151del	ENSP00000263816.3:n.2771-153_2771-151del
ENST00000443831.1:c.2360-153_2360-151del	ENSP00000409813.1:n.2360-153_2360-151del
NM_004525.2:c.2771-153_2771-151del	NP_004516.2:n.2771-153_2771-151del
XM_011511183.1:c.2771-153_2771-151del	XP_011509485.1:n.2771-153_2771-151del
XM_011511184.1:c.482-153_482-151del	XP_011509486.1:n.482-153_482-151del
XM_011511185.1:c.2771-153_2771-151del	XP_011509487.1:n.2771-153_2771-151del
NM_004525.3:c.2771-153_2771-151del MANE Select	NP_004516.2:n.2771-153_2771-151del
XM_011511183.3:c.2771-153_2771-151del	XP_011509485.1:n.2771-153_2771-151del
XM_011511184.2:c.482-153_482-151del	XP_011509486.1:n.482-153_482-151del