Canonical Allele Identifier: CA429922638

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011106A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154596A>C , CM000664.2:g.169154596A>C	GRCh38
NC_000002.11:g.170011106A>C , CM000664.1:g.170011106A>C	GRCh37
NC_000002.10:g.169719352A>C	NCBI36
NG_012634.1:g.213017T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12159T>G MANE Select	ENSP00000496870.1:p.Ser4053=
ENST00000649153.1:c.3059T>G
ENST00000650252.1:c.1187T>G	ENSP00000496887.1:p.Leu396Arg
ENST00000263816.7:c.12159T>G	ENSP00000263816.3:p.Ser4053=
NM_004525.2:c.12159T>G	NP_004516.2:p.Ser4053=
XM_011511183.1:c.12030T>G	XP_011509485.1:p.Ser4010=
XM_011511184.1:c.9870T>G	XP_011509486.1:p.Ser3290=
NM_004525.3:c.12159T>G MANE Select	NP_004516.2:p.Ser4053=
XM_011511183.3:c.12030T>G	XP_011509485.1:p.Ser4010=
XM_011511184.2:c.9870T>G	XP_011509486.1:p.Ser3290=