Canonical Allele Identifier: CA429922572

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011031A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154521A>G , CM000664.2:g.169154521A>G	GRCh38
NC_000002.11:g.170011031A>G , CM000664.1:g.170011031A>G	GRCh37
NC_000002.10:g.169719277A>G	NCBI36
NG_012634.1:g.213092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12234T>C MANE Select	ENSP00000496870.1:p.Leu4078=
ENST00000649153.1:c.3134T>C
ENST00000650252.1:c.1262T>C	ENSP00000496887.1:p.Phe421Ser
ENST00000263816.7:c.12234T>C	ENSP00000263816.3:p.Leu4078=
NM_004525.2:c.12234T>C	NP_004516.2:p.Leu4078=
XM_011511183.1:c.12105T>C	XP_011509485.1:p.Leu4035=
XM_011511184.1:c.9945T>C	XP_011509486.1:p.Leu3315=
NM_004525.3:c.12234T>C MANE Select	NP_004516.2:p.Leu4078=
XM_011511183.3:c.12105T>C	XP_011509485.1:p.Leu4035=
XM_011511184.2:c.9945T>C	XP_011509486.1:p.Leu3315=