Canonical Allele Identifier: CA381618692

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68181322T>C (hg19) ; chr11:g.68413854T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68413854T>C , CM000673.2:g.68413854T>C	GRCh38
NC_000011.9:g.68181322T>C , CM000673.1:g.68181322T>C	GRCh37
NC_000011.8:g.67937898T>C	NCBI36
NG_015835.1:g.106215T>C
NG_015835.2:g.106215T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.2669T>C MANE Select	ENSP00000294304.6:p.Met890Thr
ENST00000294304.11:c.2669T>C	ENSP00000294304.6:p.Met890Thr
ENST00000529993.5:c.*1275T>C	ENSP00000436652.1:n.*1275T>C
NM_001291902.1:c.926T>C	NP_001278831.1:p.Met309Thr
NM_002335.3:c.2669T>C	NP_002326.2:p.Met890Thr
XM_005273994.2:c.2669T>C	XP_005274051.1:p.Met890Thr
XM_011545029.1:c.2696T>C	XP_011543331.1:p.Met899Thr
XM_011545030.1:c.2696T>C	XP_011543332.1:p.Met899Thr
XM_011545031.1:c.2696T>C	XP_011543333.1:p.Met899Thr
XR_949925.1:n.2711T>C
XR_949926.1:n.2711T>C
XM_017017735.1:c.926T>C	XP_016873224.1:p.Met309Thr
XM_017017736.1:c.209T>C	XP_016873225.1:p.Met70Thr
XR_949925.2:n.2711T>C
XR_949926.2:n.2711T>C
NM_002335.4:c.2669T>C MANE Select	NP_002326.2:p.Met890Thr
NM_001291902.2:c.926T>C	NP_001278831.1:p.Met309Thr