Canonical Allele Identifier: CA381616760

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68213905T>G (hg19) ; chr11:g.68446437T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68446437T>G , CM000673.2:g.68446437T>G	GRCh38
NC_000011.9:g.68213905T>G , CM000673.1:g.68213905T>G	GRCh37
NC_000011.8:g.67970481T>G	NCBI36
NG_015835.1:g.138798T>G
NG_015835.2:g.138798T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4490T>G MANE Select	ENSP00000294304.6:p.Ile1497Ser
ENST00000294304.11:c.4490T>G	ENSP00000294304.6:p.Ile1497Ser
ENST00000529702.1:c.160T>G
ENST00000529993.5:c.*3096T>G	ENSP00000436652.1:n.*3096T>G
NM_001291902.1:c.2747T>G	NP_001278831.1:p.Ile916Ser
NM_002335.3:c.4490T>G	NP_002326.2:p.Ile1497Ser
XM_005273994.2:c.4604T>G	XP_005274051.1:p.Ile1535Ser
XM_011545029.1:c.4631T>G	XP_011543331.1:p.Ile1544Ser
XM_011545030.1:c.4517T>G	XP_011543332.1:p.Ile1506Ser
XM_011545031.1:c.4647T>G	XP_011543333.1:p.Asp1549Glu
XR_949925.1:n.4646T>G
XR_949926.1:n.4662T>G
XM_017017735.1:c.2861T>G	XP_016873224.1:p.Ile954Ser
XM_017017736.1:c.2144T>G	XP_016873225.1:p.Ile715Ser
XR_949925.2:n.4646T>G
XR_949926.2:n.4662T>G
NM_002335.4:c.4490T>G MANE Select	NP_002326.2:p.Ile1497Ser
NM_001291902.2:c.2747T>G	NP_001278831.1:p.Ile916Ser