Canonical Allele Identifier: CA349137336

Gene: LRP2

Linked Data

• gnomAD v4: 2-169154534-A-T
• MyVariant Identifiers: chr2:g.170011044A>T (hg19) ; chr2:g.169154534A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154534A>T , CM000664.2:g.169154534A>T	GRCh38
NC_000002.11:g.170011044A>T , CM000664.1:g.170011044A>T	GRCh37
NC_000002.10:g.169719290A>T	NCBI36
NG_012634.1:g.213079T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12221T>A MANE Select	ENSP00000496870.1:p.Phe4074Tyr
ENST00000649153.1:c.3121T>A
ENST00000650252.1:c.1249T>A	ENSP00000496887.1:p.Ser417Thr
ENST00000263816.7:c.12221T>A	ENSP00000263816.3:p.Phe4074Tyr
NM_004525.2:c.12221T>A	NP_004516.2:p.Phe4074Tyr
XM_011511183.1:c.12092T>A	XP_011509485.1:p.Phe4031Tyr
XM_011511184.1:c.9932T>A	XP_011509486.1:p.Phe3311Tyr
NM_004525.3:c.12221T>A MANE Select	NP_004516.2:p.Phe4074Tyr
XM_011511183.3:c.12092T>A	XP_011509485.1:p.Phe4031Tyr
XM_011511184.2:c.9932T>A	XP_011509486.1:p.Phe3311Tyr