Canonical Allele Identifier: CA1306349756
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247624_169247625delinsTC , CM000664.2:g.169247624_169247625delinsTC GRCh38
NC_000002.11:g.170104134_170104135delinsTC , CM000664.1:g.170104134_170104135delinsTC GRCh37
NC_000002.10:g.169812380_169812381delinsTC NCBI36
NG_012634.1:g.119988_119989delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2771-110_2771-109delinsGA MANE Select ENSP00000496870.1:n.2771-110_2771-109delinsGA
ENST00000263816.7:c.2771-110_2771-109delinsGA ENSP00000263816.3:n.2771-110_2771-109delinsGA
ENST00000443831.1:c.2360-110_2360-109delinsGA ENSP00000409813.1:n.2360-110_2360-109delinsGA
NM_004525.2:c.2771-110_2771-109delinsGA NP_004516.2:n.2771-110_2771-109delinsGA
XM_011511183.1:c.2771-110_2771-109delinsGA XP_011509485.1:n.2771-110_2771-109delinsGA
XM_011511184.1:c.482-110_482-109delinsGA XP_011509486.1:n.482-110_482-109delinsGA
XM_011511185.1:c.2771-110_2771-109delinsGA XP_011509487.1:n.2771-110_2771-109delinsGA
NM_004525.3:c.2771-110_2771-109delinsGA MANE Select NP_004516.2:n.2771-110_2771-109delinsGA
XM_011511183.3:c.2771-110_2771-109delinsGA XP_011509485.1:n.2771-110_2771-109delinsGA
XM_011511184.2:c.482-110_482-109delinsGA XP_011509486.1:n.482-110_482-109delinsGA