Canonical Allele Identifier: CA429922540
Gene: LRP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.170010971G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154461G>C , CM000664.2:g.169154461G>C GRCh38
NC_000002.11:g.170010971G>C , CM000664.1:g.170010971G>C GRCh37
NC_000002.10:g.169719217G>C NCBI36
NG_012634.1:g.213152C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12294C>G MANE Select ENSP00000496870.1:p.Leu4098=
ENST00000649153.1:c.3194C>G
ENST00000650252.1:c.1322C>G ENSP00000496887.1:n.1322C>G
ENST00000263816.7:c.12294C>G ENSP00000263816.3:p.Leu4098=
NM_004525.2:c.12294C>G NP_004516.2:p.Leu4098=
XM_011511183.1:c.12165C>G XP_011509485.1:p.Leu4055=
XM_011511184.1:c.10005C>G XP_011509486.1:p.Leu3335=
NM_004525.3:c.12294C>G MANE Select NP_004516.2:p.Leu4098=
XM_011511183.3:c.12165C>G XP_011509485.1:p.Leu4055=
XM_011511184.2:c.10005C>G XP_011509486.1:p.Leu3335=