Canonical Allele Identifier: CA349136894

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170010970T>A (hg19) ; chr2:g.169154460T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154460T>A , CM000664.2:g.169154460T>A	GRCh38
NC_000002.11:g.170010970T>A , CM000664.1:g.170010970T>A	GRCh37
NC_000002.10:g.169719216T>A	NCBI36
NG_012634.1:g.213153A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12295A>T MANE Select	ENSP00000496870.1:p.Ser4099Cys
ENST00000649153.1:c.3195A>T
ENST00000650252.1:c.1323A>T	ENSP00000496887.1:n.1323A>T
ENST00000263816.7:c.12295A>T	ENSP00000263816.3:p.Ser4099Cys
NM_004525.2:c.12295A>T	NP_004516.2:p.Ser4099Cys
XM_011511183.1:c.12166A>T	XP_011509485.1:p.Ser4056Cys
XM_011511184.1:c.10006A>T	XP_011509486.1:p.Ser3336Cys
NM_004525.3:c.12295A>T MANE Select	NP_004516.2:p.Ser4099Cys
XM_011511183.3:c.12166A>T	XP_011509485.1:p.Ser4056Cys
XM_011511184.2:c.10006A>T	XP_011509486.1:p.Ser3336Cys