Canonical Allele Identifier: CA1306349645
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247372A= , CM000664.2:g.169247372A= GRCh38
NC_000002.11:g.170103882A= , CM000664.1:g.170103882A= GRCh37
NC_000002.10:g.169812128A= NCBI36
NG_012634.1:g.120241T=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2908+6T= MANE Select ENSP00000496870.1:n.2908+6T=
ENST00000263816.7:c.2908+6T= ENSP00000263816.3:n.2908+6T=
ENST00000443831.1:c.2497+6T= ENSP00000409813.1:n.2497+6T=
NM_004525.2:c.2908+6T= NP_004516.2:n.2908+6T=
XM_011511183.1:c.2908+6T= XP_011509485.1:n.2908+6T=
XM_011511184.1:c.619+6T= XP_011509486.1:n.619+6T=
XM_011511185.1:c.2908+6T= XP_011509487.1:n.2908+6T=
NM_004525.3:c.2908+6T= MANE Select NP_004516.2:n.2908+6T=
XM_011511183.3:c.2908+6T= XP_011509485.1:n.2908+6T=
XM_011511184.2:c.619+6T= XP_011509486.1:n.619+6T=