Canonical Allele Identifier: CA381615790

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68174214A>T (hg19) ; chr11:g.68406746A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406746A>T , CM000673.2:g.68406746A>T	GRCh38
NC_000011.9:g.68174214A>T , CM000673.1:g.68174214A>T	GRCh37
NC_000011.8:g.67930790A>T	NCBI36
NG_015835.1:g.99107A>T
NG_015835.2:g.99107A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.2024A>T MANE Select	ENSP00000294304.6:p.Lys675Met
ENST00000294304.11:c.2024A>T	ENSP00000294304.6:p.Lys675Met
ENST00000529993.5:c.*630A>T	ENSP00000436652.1:n.*630A>T
NM_001291902.1:c.281A>T	NP_001278831.1:p.Lys94Met
NM_002335.3:c.2024A>T	NP_002326.2:p.Lys675Met
XM_005273994.2:c.2024A>T	XP_005274051.1:p.Lys675Met
XM_011545029.1:c.2051A>T	XP_011543331.1:p.Lys684Met
XM_011545030.1:c.2051A>T	XP_011543332.1:p.Lys684Met
XM_011545031.1:c.2051A>T	XP_011543333.1:p.Lys684Met
XR_949925.1:n.2066A>T
XR_949926.1:n.2066A>T
XM_017017735.1:c.281A>T	XP_016873224.1:p.Lys94Met
XR_001747874.1:n.2066A>T
XR_949925.2:n.2066A>T
XR_949926.2:n.2066A>T
NM_002335.4:c.2024A>T MANE Select	NP_002326.2:p.Lys675Met
NM_001291902.2:c.281A>T	NP_001278831.1:p.Lys94Met