Canonical Allele Identifier: CA1306349775

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247665_169247668delinsCACG , CM000664.2:g.169247665_169247668delinsCACG	GRCh38
NC_000002.11:g.170104175_170104178delinsCACG , CM000664.1:g.170104175_170104178delinsCACG	GRCh37
NC_000002.10:g.169812421_169812424delinsCACG	NCBI36
NG_012634.1:g.119945_119948delinsCGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2771-153_2771-150delinsCGTG MANE Select	ENSP00000496870.1:n.2771-153_2771-150delinsCGTG
ENST00000263816.7:c.2771-153_2771-150delinsCGTG	ENSP00000263816.3:n.2771-153_2771-150delinsCGTG
ENST00000443831.1:c.2360-153_2360-150delinsCGTG	ENSP00000409813.1:n.2360-153_2360-150delinsCGTG
NM_004525.2:c.2771-153_2771-150delinsCGTG	NP_004516.2:n.2771-153_2771-150delinsCGTG
XM_011511183.1:c.2771-153_2771-150delinsCGTG	XP_011509485.1:n.2771-153_2771-150delinsCGTG
XM_011511184.1:c.482-153_482-150delinsCGTG	XP_011509486.1:n.482-153_482-150delinsCGTG
XM_011511185.1:c.2771-153_2771-150delinsCGTG	XP_011509487.1:n.2771-153_2771-150delinsCGTG
NM_004525.3:c.2771-153_2771-150delinsCGTG MANE Select	NP_004516.2:n.2771-153_2771-150delinsCGTG
XM_011511183.3:c.2771-153_2771-150delinsCGTG	XP_011509485.1:n.2771-153_2771-150delinsCGTG
XM_011511184.2:c.482-153_482-150delinsCGTG	XP_011509486.1:n.482-153_482-150delinsCGTG