Canonical Allele Identifier: CA1955177

Gene: LRP2

Linked Data

• dbSNP Id: rs752754038
• ExAC: 2:170103853 C / CA
• gnomAD v2: 2-170103853-C-CA
• gnomAD v3: 2-169247343-C-CA
• gnomAD v4: 2-169247343-C-CA
• MyVariant Identifiers: chr2:g.170103854_170103855insA (hg19) ; chr2:g.170103853_170103854insA (hg19) ; chr2:g.169247343_169247344insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247350dup , CM000664.2:g.169247350dup	GRCh38
NC_000002.11:g.170103860dup , CM000664.1:g.170103860dup	GRCh37
NC_000002.10:g.169812106dup	NCBI36
NG_012634.1:g.120269dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.2908+34dup MANE Select	ENSP00000496870.1:n.2908+34dup
ENST00000263816.7:c.2908+34dup	ENSP00000263816.3:n.2908+34dup
ENST00000443831.1:c.2497+34dup	ENSP00000409813.1:n.2497+34dup
NM_004525.2:c.2908+34dup	NP_004516.2:n.2908+34dup
XM_011511183.1:c.2908+34dup	XP_011509485.1:n.2908+34dup
XM_011511184.1:c.619+34dup	XP_011509486.1:n.619+34dup
XM_011511185.1:c.2908+34dup	XP_011509487.1:n.2908+34dup
NM_004525.3:c.2908+34dup MANE Select	NP_004516.2:n.2908+34dup
XM_011511183.3:c.2908+34dup	XP_011509485.1:n.2908+34dup
XM_011511184.2:c.619+34dup	XP_011509486.1:n.619+34dup