Canonical Allele Identifier: CA429917409

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.169985580A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169129070A>G , CM000664.2:g.169129070A>G	GRCh38
NC_000002.11:g.169985580A>G , CM000664.1:g.169985580A>G	GRCh37
NC_000002.10:g.169693826A>G	NCBI36
NG_012634.1:g.238543T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13743T>C MANE Select	ENSP00000496870.1:p.Asn4581=
ENST00000649153.1:c.4552T>C
ENST00000650252.1:c.2734T>C	ENSP00000496887.1:n.2734T>C
ENST00000263816.7:c.13743T>C	ENSP00000263816.3:p.Asn4581=
NM_004525.2:c.13743T>C	NP_004516.2:p.Asn4581=
XM_011511183.1:c.13614T>C	XP_011509485.1:p.Asn4538=
XM_011511184.1:c.11454T>C	XP_011509486.1:p.Asn3818=
NM_004525.3:c.13743T>C MANE Select	NP_004516.2:p.Asn4581=
XM_011511183.3:c.13614T>C	XP_011509485.1:p.Asn4538=
XM_011511184.2:c.11454T>C	XP_011509486.1:p.Asn3818=