Canonical Allele Identifier: CA429921006

Gene: LRP2

Linked Data

• gnomAD v4: 2-169259087-C-G
• MyVariant Identifiers: chr2:g.170115597C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259087C>G , CM000664.2:g.169259087C>G	GRCh38
NC_000002.11:g.170115597C>G , CM000664.1:g.170115597C>G	GRCh37
NC_000002.10:g.169823843C>G	NCBI36
NG_012634.1:g.108526G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2451G>C MANE Select	ENSP00000496870.1:p.Thr817=
ENST00000263816.7:c.2451G>C	ENSP00000263816.3:p.Thr817=
ENST00000443831.1:c.2040G>C	ENSP00000409813.1:p.Thr680=
NM_004525.2:c.2451G>C	NP_004516.2:p.Thr817=
XM_011511183.1:c.2451G>C	XP_011509485.1:p.Thr817=
XM_011511184.1:c.162G>C	XP_011509486.1:p.Thr54=
XM_011511185.1:c.2451G>C	XP_011509487.1:p.Thr817=
NM_004525.3:c.2451G>C MANE Select	NP_004516.2:p.Thr817=
XM_011511183.3:c.2451G>C	XP_011509485.1:p.Thr817=
XM_011511184.2:c.162G>C	XP_011509486.1:p.Thr54=