Canonical Allele Identifier: CA349158597

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170115685C>A (hg19) ; chr2:g.169259175C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259175C>A , CM000664.2:g.169259175C>A	GRCh38
NC_000002.11:g.170115685C>A , CM000664.1:g.170115685C>A	GRCh37
NC_000002.10:g.169823931C>A	NCBI36
NG_012634.1:g.108438G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2363G>T MANE Select	ENSP00000496870.1:p.Ser788Ile
ENST00000263816.7:c.2363G>T	ENSP00000263816.3:p.Ser788Ile
ENST00000443831.1:c.1952G>T	ENSP00000409813.1:p.Ser651Ile
NM_004525.2:c.2363G>T	NP_004516.2:p.Ser788Ile
XM_011511183.1:c.2363G>T	XP_011509485.1:p.Ser788Ile
XM_011511184.1:c.74G>T	XP_011509486.1:p.Ser25Ile
XM_011511185.1:c.2363G>T	XP_011509487.1:p.Ser788Ile
NM_004525.3:c.2363G>T MANE Select	NP_004516.2:p.Ser788Ile
XM_011511183.3:c.2363G>T	XP_011509485.1:p.Ser788Ile
XM_011511184.2:c.74G>T	XP_011509486.1:p.Ser25Ile