Canonical Allele Identifier: CA349137179

Gene: LRP2

Linked Data

• dbSNP Id: rs1686261544
• MyVariant Identifiers: chr2:g.170011018A>T (hg19) ; chr2:g.169154508A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154508A>T , CM000664.2:g.169154508A>T	GRCh38
NC_000002.11:g.170011018A>T , CM000664.1:g.170011018A>T	GRCh37
NC_000002.10:g.169719264A>T	NCBI36
NG_012634.1:g.213105T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12247T>A MANE Select	ENSP00000496870.1:p.Tyr4083Asn
ENST00000649153.1:c.3147T>A
ENST00000650252.1:c.1275T>A	ENSP00000496887.1:p.Asn425Lys
ENST00000263816.7:c.12247T>A	ENSP00000263816.3:p.Tyr4083Asn
NM_004525.2:c.12247T>A	NP_004516.2:p.Tyr4083Asn
XM_011511183.1:c.12118T>A	XP_011509485.1:p.Tyr4040Asn
XM_011511184.1:c.9958T>A	XP_011509486.1:p.Tyr3320Asn
NM_004525.3:c.12247T>A MANE Select	NP_004516.2:p.Tyr4083Asn
XM_011511183.3:c.12118T>A	XP_011509485.1:p.Tyr4040Asn
XM_011511184.2:c.9958T>A	XP_011509486.1:p.Tyr3320Asn