Canonical Allele Identifier: CA349158445

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170115646G>A (hg19) ; chr2:g.169259136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259136G>A , CM000664.2:g.169259136G>A	GRCh38
NC_000002.11:g.170115646G>A , CM000664.1:g.170115646G>A	GRCh37
NC_000002.10:g.169823892G>A	NCBI36
NG_012634.1:g.108477C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2402C>T MANE Select	ENSP00000496870.1:p.Thr801Ile
ENST00000263816.7:c.2402C>T	ENSP00000263816.3:p.Thr801Ile
ENST00000443831.1:c.1991C>T	ENSP00000409813.1:p.Thr664Ile
NM_004525.2:c.2402C>T	NP_004516.2:p.Thr801Ile
XM_011511183.1:c.2402C>T	XP_011509485.1:p.Thr801Ile
XM_011511184.1:c.113C>T	XP_011509486.1:p.Thr38Ile
XM_011511185.1:c.2402C>T	XP_011509487.1:p.Thr801Ile
NM_004525.3:c.2402C>T MANE Select	NP_004516.2:p.Thr801Ile
XM_011511183.3:c.2402C>T	XP_011509485.1:p.Thr801Ile
XM_011511184.2:c.113C>T	XP_011509486.1:p.Thr38Ile