Canonical Allele Identifier: CA1306353641

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169258884_169258888delinsGAAAT , CM000664.2:g.169258884_169258888delinsGAAAT	GRCh38
NC_000002.11:g.170115394_170115398delinsGAAAT , CM000664.1:g.170115394_170115398delinsGAAAT	GRCh37
NC_000002.10:g.169823640_169823644delinsGAAAT	NCBI36
NG_012634.1:g.108725_108729delinsATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2513+137_2513+141delinsATTTC MANE Select	ENSP00000496870.1:n.2513+137_2513+141delinsATTTC
ENST00000263816.7:c.2513+137_2513+141delinsATTTC	ENSP00000263816.3:n.2513+137_2513+141delinsATTTC
ENST00000443831.1:c.2102+137_2102+141delinsATTTC	ENSP00000409813.1:n.2102+137_2102+141delinsATTTC
NM_004525.2:c.2513+137_2513+141delinsATTTC	NP_004516.2:n.2513+137_2513+141delinsATTTC
XM_011511183.1:c.2513+137_2513+141delinsATTTC	XP_011509485.1:n.2513+137_2513+141delinsATTTC
XM_011511184.1:c.224+137_224+141delinsATTTC	XP_011509486.1:n.224+137_224+141delinsATTTC
XM_011511185.1:c.2513+137_2513+141delinsATTTC	XP_011509487.1:n.2513+137_2513+141delinsATTTC
NM_004525.3:c.2513+137_2513+141delinsATTTC MANE Select	NP_004516.2:n.2513+137_2513+141delinsATTTC
XM_011511183.3:c.2513+137_2513+141delinsATTTC	XP_011509485.1:n.2513+137_2513+141delinsATTTC
XM_011511184.2:c.224+137_224+141delinsATTTC	XP_011509486.1:n.224+137_224+141delinsATTTC