Canonical Allele Identifier: CA349136897
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154460T>C , CM000664.2:g.169154460T>C GRCh38
NC_000002.11:g.170010970T>C , CM000664.1:g.170010970T>C GRCh37
NC_000002.10:g.169719216T>C NCBI36
NG_012634.1:g.213153A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295A>G MANE Select ENSP00000496870.1:p.Ser4099Gly
ENST00000649153.1:c.3195A>G
ENST00000650252.1:c.1323A>G ENSP00000496887.1:n.1323A>G
ENST00000263816.7:c.12295A>G ENSP00000263816.3:p.Ser4099Gly
NM_004525.2:c.12295A>G NP_004516.2:p.Ser4099Gly
XM_011511183.1:c.12166A>G XP_011509485.1:p.Ser4056Gly
XM_011511184.1:c.10006A>G XP_011509486.1:p.Ser3336Gly
NM_004525.3:c.12295A>G MANE Select NP_004516.2:p.Ser4099Gly
XM_011511183.3:c.12166A>G XP_011509485.1:p.Ser4056Gly
XM_011511184.2:c.10006A>G XP_011509486.1:p.Ser3336Gly