Canonical Allele Identifier: CA1306353862

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259344_169259346delinsTTA , CM000664.2:g.169259344_169259346delinsTTA	GRCh38
NC_000002.11:g.170115854_170115856delinsTTA , CM000664.1:g.170115854_170115856delinsTTA	GRCh37
NC_000002.10:g.169824100_169824102delinsTTA	NCBI36
NG_012634.1:g.108267_108269delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-129_2321-127delinsTAA MANE Select	ENSP00000496870.1:n.2321-129_2321-127delinsTAA
ENST00000263816.7:c.2321-129_2321-127delinsTAA	ENSP00000263816.3:n.2321-129_2321-127delinsTAA
ENST00000443831.1:c.1910-129_1910-127delinsTAA	ENSP00000409813.1:n.1910-129_1910-127delinsTAA
NM_004525.2:c.2321-129_2321-127delinsTAA	NP_004516.2:n.2321-129_2321-127delinsTAA
XM_011511183.1:c.2321-129_2321-127delinsTAA	XP_011509485.1:n.2321-129_2321-127delinsTAA
XM_011511184.1:c.32-129_32-127delinsTAA	XP_011509486.1:n.32-129_32-127delinsTAA
XM_011511185.1:c.2321-129_2321-127delinsTAA	XP_011509487.1:n.2321-129_2321-127delinsTAA
NM_004525.3:c.2321-129_2321-127delinsTAA MANE Select	NP_004516.2:n.2321-129_2321-127delinsTAA
XM_011511183.3:c.2321-129_2321-127delinsTAA	XP_011509485.1:n.2321-129_2321-127delinsTAA
XM_011511184.2:c.32-129_32-127delinsTAA	XP_011509486.1:n.32-129_32-127delinsTAA