Canonical Allele Identifier: CA2700932910

Gene: LRP2

Linked Data

• dbSNP Id: rs2105358597

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154368_169154387del , CM000664.2:g.169154368_169154387del	GRCh38
NC_000002.11:g.170010878_170010897del , CM000664.1:g.170010878_170010897del	GRCh37
NC_000002.10:g.169719124_169719143del	NCBI36
NG_012634.1:g.213232_213251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12295+79_12295+98del MANE Select	ENSP00000496870.1:n.12295+79_12295+98del
ENST00000649153.1:c.3195+79_3195+98del
ENST00000650252.1:c.1323+79_1323+98del	ENSP00000496887.1:n.1323+79_1323+98del
ENST00000263816.7:c.12295+79_12295+98del	ENSP00000263816.3:n.12295+79_12295+98del
NM_004525.2:c.12295+79_12295+98del	NP_004516.2:n.12295+79_12295+98del
XM_011511183.1:c.12166+79_12166+98del	XP_011509485.1:n.12166+79_12166+98del
XM_011511184.1:c.10006+79_10006+98del	XP_011509486.1:n.10006+79_10006+98del
NM_004525.3:c.12295+79_12295+98del MANE Select	NP_004516.2:n.12295+79_12295+98del
XM_011511183.3:c.12166+79_12166+98del	XP_011509485.1:n.12166+79_12166+98del
XM_011511184.2:c.10006+79_10006+98del	XP_011509486.1:n.10006+79_10006+98del