Canonical Allele Identifier: CA1306353755
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259108G= , CM000664.2:g.169259108G= GRCh38
NC_000002.11:g.170115618G= , CM000664.1:g.170115618G= GRCh37
NC_000002.10:g.169823864G= NCBI36
NG_012634.1:g.108505C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2430C= MANE Select ENSP00000496870.1:p.Val810=
ENST00000263816.7:c.2430C= ENSP00000263816.3:p.Val810=
ENST00000443831.1:c.2019C= ENSP00000409813.1:p.Val673=
NM_004525.2:c.2430C= NP_004516.2:p.Val810=
XM_011511183.1:c.2430C= XP_011509485.1:p.Val810=
XM_011511184.1:c.141C= XP_011509486.1:p.Val47=
XM_011511185.1:c.2430C= XP_011509487.1:p.Val810=
NM_004525.3:c.2430C= MANE Select NP_004516.2:p.Val810=
XM_011511183.3:c.2430C= XP_011509485.1:p.Val810=
XM_011511184.2:c.141C= XP_011509486.1:p.Val47=