Canonical Allele Identifier: CA349137483

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011083T>A (hg19) ; chr2:g.169154573T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154573T>A , CM000664.2:g.169154573T>A	GRCh38
NC_000002.11:g.170011083T>A , CM000664.1:g.170011083T>A	GRCh37
NC_000002.10:g.169719329T>A	NCBI36
NG_012634.1:g.213040A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12182A>T MANE Select	ENSP00000496870.1:p.Asn4061Ile
ENST00000649153.1:c.3082A>T
ENST00000650252.1:c.1210A>T	ENSP00000496887.1:p.Met404Leu
ENST00000263816.7:c.12182A>T	ENSP00000263816.3:p.Asn4061Ile
NM_004525.2:c.12182A>T	NP_004516.2:p.Asn4061Ile
XM_011511183.1:c.12053A>T	XP_011509485.1:p.Asn4018Ile
XM_011511184.1:c.9893A>T	XP_011509486.1:p.Asn3298Ile
NM_004525.3:c.12182A>T MANE Select	NP_004516.2:p.Asn4061Ile
XM_011511183.3:c.12053A>T	XP_011509485.1:p.Asn4018Ile
XM_011511184.2:c.9893A>T	XP_011509486.1:p.Asn3298Ile