Canonical Allele Identifier: CA349158450
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259137T>A , CM000664.2:g.169259137T>A GRCh38
NC_000002.11:g.170115647T>A , CM000664.1:g.170115647T>A GRCh37
NC_000002.10:g.169823893T>A NCBI36
NG_012634.1:g.108476A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2401A>T MANE Select ENSP00000496870.1:p.Thr801Ser
ENST00000263816.7:c.2401A>T ENSP00000263816.3:p.Thr801Ser
ENST00000443831.1:c.1990A>T ENSP00000409813.1:p.Thr664Ser
NM_004525.2:c.2401A>T NP_004516.2:p.Thr801Ser
XM_011511183.1:c.2401A>T XP_011509485.1:p.Thr801Ser
XM_011511184.1:c.112A>T XP_011509486.1:p.Thr38Ser
XM_011511185.1:c.2401A>T XP_011509487.1:p.Thr801Ser
NM_004525.3:c.2401A>T MANE Select NP_004516.2:p.Thr801Ser
XM_011511183.3:c.2401A>T XP_011509485.1:p.Thr801Ser
XM_011511184.2:c.112A>T XP_011509486.1:p.Thr38Ser