Canonical Allele Identifier: CA349158403
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259125A>T , CM000664.2:g.169259125A>T GRCh38
NC_000002.11:g.170115635A>T , CM000664.1:g.170115635A>T GRCh37
NC_000002.10:g.169823881A>T NCBI36
NG_012634.1:g.108488T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2413T>A MANE Select ENSP00000496870.1:p.Tyr805Asn
ENST00000263816.7:c.2413T>A ENSP00000263816.3:p.Tyr805Asn
ENST00000443831.1:c.2002T>A ENSP00000409813.1:p.Tyr668Asn
NM_004525.2:c.2413T>A NP_004516.2:p.Tyr805Asn
XM_011511183.1:c.2413T>A XP_011509485.1:p.Tyr805Asn
XM_011511184.1:c.124T>A XP_011509486.1:p.Tyr42Asn
XM_011511185.1:c.2413T>A XP_011509487.1:p.Tyr805Asn
NM_004525.3:c.2413T>A MANE Select NP_004516.2:p.Tyr805Asn
XM_011511183.3:c.2413T>A XP_011509485.1:p.Tyr805Asn
XM_011511184.2:c.124T>A XP_011509486.1:p.Tyr42Asn