Canonical Allele Identifier: CA1306305482

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154371_169154374delinsCATT , CM000664.2:g.169154371_169154374delinsCATT	GRCh38
NC_000002.11:g.170010881_170010884delinsCATT , CM000664.1:g.170010881_170010884delinsCATT	GRCh37
NC_000002.10:g.169719127_169719130delinsCATT	NCBI36
NG_012634.1:g.213239_213242delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12295+86_12295+89delinsAATG MANE Select	ENSP00000496870.1:n.12295+86_12295+89delinsAATG
ENST00000649153.1:c.3195+86_3195+89delinsAATG
ENST00000650252.1:c.1323+86_1323+89delinsAATG	ENSP00000496887.1:n.1323+86_1323+89delinsAATG
ENST00000263816.7:c.12295+86_12295+89delinsAATG	ENSP00000263816.3:n.12295+86_12295+89delinsAATG
NM_004525.2:c.12295+86_12295+89delinsAATG	NP_004516.2:n.12295+86_12295+89delinsAATG
XM_011511183.1:c.12166+86_12166+89delinsAATG	XP_011509485.1:n.12166+86_12166+89delinsAATG
XM_011511184.1:c.10006+86_10006+89delinsAATG	XP_011509486.1:n.10006+86_10006+89delinsAATG
NM_004525.3:c.12295+86_12295+89delinsAATG MANE Select	NP_004516.2:n.12295+86_12295+89delinsAATG
XM_011511183.3:c.12166+86_12166+89delinsAATG	XP_011509485.1:n.12166+86_12166+89delinsAATG
XM_011511184.2:c.10006+86_10006+89delinsAATG	XP_011509486.1:n.10006+86_10006+89delinsAATG