Canonical Allele Identifier: CA349137338

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011044A>G (hg19) ; chr2:g.169154534A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12221T>C MANE Select	ENSP00000496870.1:p.Phe4074Ser
ENST00000649153.1:c.3121T>C
ENST00000650252.1:c.1249T>C	ENSP00000496887.1:p.Ser417Pro
ENST00000263816.7:c.12221T>C	ENSP00000263816.3:p.Phe4074Ser
NM_004525.2:c.12221T>C	NP_004516.2:p.Phe4074Ser
XM_011511183.1:c.12092T>C	XP_011509485.1:p.Phe4031Ser
XM_011511184.1:c.9932T>C	XP_011509486.1:p.Phe3311Ser
NM_004525.3:c.12221T>C MANE Select	NP_004516.2:p.Phe4074Ser
XM_011511183.3:c.12092T>C	XP_011509485.1:p.Phe4031Ser
XM_011511184.2:c.9932T>C	XP_011509486.1:p.Phe3311Ser