Canonical Allele Identifier: CA59921270

Gene: LRP2

Linked Data

• dbSNP Id: rs757316938
• MyVariant Identifiers: chr2:g.170116077_170116078insCCACC (hg19) ; chr2:g.169259567_169259568insCCACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259569_169259573dup , CM000664.2:g.169259569_169259573dup	GRCh38
NC_000002.11:g.170116079_170116083dup , CM000664.1:g.170116079_170116083dup	GRCh37
NC_000002.10:g.169824325_169824329dup	NCBI36
NG_012634.1:g.108041_108045dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-355_2321-351dup MANE Select	ENSP00000496870.1:n.2321-355_2321-351dup
ENST00000263816.7:c.2321-355_2321-351dup	ENSP00000263816.3:n.2321-355_2321-351dup
ENST00000443831.1:c.1910-355_1910-351dup	ENSP00000409813.1:n.1910-355_1910-351dup
NM_004525.2:c.2321-355_2321-351dup	NP_004516.2:n.2321-355_2321-351dup
XM_011511183.1:c.2321-355_2321-351dup	XP_011509485.1:n.2321-355_2321-351dup
XM_011511184.1:c.32-355_32-351dup	XP_011509486.1:n.32-355_32-351dup
XM_011511185.1:c.2321-355_2321-351dup	XP_011509487.1:n.2321-355_2321-351dup
NM_004525.3:c.2321-355_2321-351dup MANE Select	NP_004516.2:n.2321-355_2321-351dup
XM_011511183.3:c.2321-355_2321-351dup	XP_011509485.1:n.2321-355_2321-351dup
XM_011511184.2:c.32-355_32-351dup	XP_011509486.1:n.32-355_32-351dup