Canonical Allele Identifier: CA349149404

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.169985571T>G (hg19) ; chr2:g.169129061T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169129061T>G , CM000664.2:g.169129061T>G	GRCh38
NC_000002.11:g.169985571T>G , CM000664.1:g.169985571T>G	GRCh37
NC_000002.10:g.169693817T>G	NCBI36
NG_012634.1:g.238552A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13752A>C MANE Select	ENSP00000496870.1:p.Lys4584Asn
ENST00000649153.1:c.4561A>C
ENST00000650252.1:c.2743A>C	ENSP00000496887.1:n.2743A>C
ENST00000263816.7:c.13752A>C	ENSP00000263816.3:p.Lys4584Asn
NM_004525.2:c.13752A>C	NP_004516.2:p.Lys4584Asn
XM_011511183.1:c.13623A>C	XP_011509485.1:p.Lys4541Asn
XM_011511184.1:c.11463A>C	XP_011509486.1:p.Lys3821Asn
NM_004525.3:c.13752A>C MANE Select	NP_004516.2:p.Lys4584Asn
XM_011511183.3:c.13623A>C	XP_011509485.1:p.Lys4541Asn
XM_011511184.2:c.11463A>C	XP_011509486.1:p.Lys3821Asn