Canonical Allele Identifier: CA381616383

Gene: LRP5

Linked Data

• gnomAD v4: 11-68409974-G-T
• MyVariant Identifiers: chr11:g.68177442G>T (hg19) ; chr11:g.68409974G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68409974G>T , CM000673.2:g.68409974G>T	GRCh38
NC_000011.9:g.68177442G>T , CM000673.1:g.68177442G>T	GRCh37
NC_000011.8:g.67934018G>T	NCBI36
NG_015835.1:g.102335G>T
NG_015835.2:g.102335G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.2152G>T MANE Select	ENSP00000294304.6:p.Asp718Tyr
ENST00000294304.11:c.2152G>T	ENSP00000294304.6:p.Asp718Tyr
ENST00000529993.5:c.*758G>T	ENSP00000436652.1:n.*758G>T
NM_001291902.1:c.409G>T	NP_001278831.1:p.Asp137Tyr
NM_002335.3:c.2152G>T	NP_002326.2:p.Asp718Tyr
XM_005273994.2:c.2152G>T	XP_005274051.1:p.Asp718Tyr
XM_011545029.1:c.2179G>T	XP_011543331.1:p.Asp727Tyr
XM_011545030.1:c.2179G>T	XP_011543332.1:p.Asp727Tyr
XM_011545031.1:c.2179G>T	XP_011543333.1:p.Asp727Tyr
XR_949925.1:n.2194G>T
XR_949926.1:n.2194G>T
XM_017017735.1:c.409G>T	XP_016873224.1:p.Asp137Tyr
XR_001747874.1:n.2194G>T
XR_949925.2:n.2194G>T
XR_949926.2:n.2194G>T
NM_002335.4:c.2152G>T MANE Select	NP_002326.2:p.Asp718Tyr
NM_001291902.2:c.409G>T	NP_001278831.1:p.Asp137Tyr