Canonical Allele Identifier: CA1306353945

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259457_169259458delinsCA , CM000664.2:g.169259457_169259458delinsCA	GRCh38
NC_000002.11:g.170115967_170115968delinsCA , CM000664.1:g.170115967_170115968delinsCA	GRCh37
NC_000002.10:g.169824213_169824214delinsCA	NCBI36
NG_012634.1:g.108155_108156delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-241_2321-240delinsTG MANE Select	ENSP00000496870.1:n.2321-241_2321-240delinsTG
ENST00000263816.7:c.2321-241_2321-240delinsTG	ENSP00000263816.3:n.2321-241_2321-240delinsTG
ENST00000443831.1:c.1910-241_1910-240delinsTG	ENSP00000409813.1:n.1910-241_1910-240delinsTG
NM_004525.2:c.2321-241_2321-240delinsTG	NP_004516.2:n.2321-241_2321-240delinsTG
XM_011511183.1:c.2321-241_2321-240delinsTG	XP_011509485.1:n.2321-241_2321-240delinsTG
XM_011511184.1:c.32-241_32-240delinsTG	XP_011509486.1:n.32-241_32-240delinsTG
XM_011511185.1:c.2321-241_2321-240delinsTG	XP_011509487.1:n.2321-241_2321-240delinsTG
NM_004525.3:c.2321-241_2321-240delinsTG MANE Select	NP_004516.2:n.2321-241_2321-240delinsTG
XM_011511183.3:c.2321-241_2321-240delinsTG	XP_011509485.1:n.2321-241_2321-240delinsTG
XM_011511184.2:c.32-241_32-240delinsTG	XP_011509486.1:n.32-241_32-240delinsTG