Canonical Allele Identifier: CA429922602

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011076T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154566T>A , CM000664.2:g.169154566T>A	GRCh38
NC_000002.11:g.170011076T>A , CM000664.1:g.170011076T>A	GRCh37
NC_000002.10:g.169719322T>A	NCBI36
NG_012634.1:g.213047A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12189A>T MANE Select	ENSP00000496870.1:p.Arg4063=
ENST00000649153.1:c.3089A>T
ENST00000650252.1:c.1217A>T	ENSP00000496887.1:p.Glu406Val
ENST00000263816.7:c.12189A>T	ENSP00000263816.3:p.Arg4063=
NM_004525.2:c.12189A>T	NP_004516.2:p.Arg4063=
XM_011511183.1:c.12060A>T	XP_011509485.1:p.Arg4020=
XM_011511184.1:c.9900A>T	XP_011509486.1:p.Arg3300=
NM_004525.3:c.12189A>T MANE Select	NP_004516.2:p.Arg4063=
XM_011511183.3:c.12060A>T	XP_011509485.1:p.Arg4020=
XM_011511184.2:c.9900A>T	XP_011509486.1:p.Arg3300=