Canonical Allele Identifier: CA429922552
Gene: LRP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.170010989A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154479A>G , CM000664.2:g.169154479A>G GRCh38
NC_000002.11:g.170010989A>G , CM000664.1:g.170010989A>G GRCh37
NC_000002.10:g.169719235A>G NCBI36
NG_012634.1:g.213134T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12276T>C MANE Select ENSP00000496870.1:p.Asp4092=
ENST00000649153.1:c.3176T>C
ENST00000650252.1:c.1304T>C ENSP00000496887.1:p.Ile435Thr
ENST00000263816.7:c.12276T>C ENSP00000263816.3:p.Asp4092=
NM_004525.2:c.12276T>C NP_004516.2:p.Asp4092=
XM_011511183.1:c.12147T>C XP_011509485.1:p.Asp4049=
XM_011511184.1:c.9987T>C XP_011509486.1:p.Asp3329=
NM_004525.3:c.12276T>C MANE Select NP_004516.2:p.Asp4092=
XM_011511183.3:c.12147T>C XP_011509485.1:p.Asp4049=
XM_011511184.2:c.9987T>C XP_011509486.1:p.Asp3329=