Canonical Allele Identifier: CA6148935

Gene: LRP5

Linked Data

• ClinVar Variation Id: 2961977
• ClinVar RCV Id: RCV003822623
• dbSNP Id: rs771043544
• ExAC: 11:68115433 C / T
• gnomAD v2: 11-68115433-C-T
• gnomAD v3: 11-68347965-C-T
• gnomAD v4: 11-68347965-C-T
• MyVariant Identifiers: chr11:g.68115433C>T (hg19) ; chr11:g.68347965C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68347965C>T , CM000673.2:g.68347965C>T	GRCh38
NC_000011.9:g.68115433C>T , CM000673.1:g.68115433C>T	GRCh37
NC_000011.8:g.67872009C>T	NCBI36
NG_015835.1:g.40326C>T
NG_015835.2:g.40326C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.210C>T MANE Select	ENSP00000294304.6:p.Phe70=
ENST00000294304.11:c.210C>T	ENSP00000294304.6:p.Phe70=
ENST00000529993.5:c.210C>T	ENSP00000436652.1:p.Phe70=
NM_001291902.1:c.-1556C>T	NP_001278831.1:n.-1556C>T
NM_002335.3:c.210C>T	NP_002326.2:p.Phe70=
XM_005273994.2:c.210C>T	XP_005274051.1:p.Phe70=
XM_011545029.1:c.237C>T	XP_011543331.1:p.Phe79=
XM_011545030.1:c.237C>T	XP_011543332.1:p.Phe79=
XM_011545031.1:c.237C>T	XP_011543333.1:p.Phe79=
XR_949925.1:n.252C>T
XR_949926.1:n.252C>T
XR_001747874.1:n.252C>T
XR_949925.2:n.252C>T
XR_949926.2:n.252C>T
NM_002335.4:c.210C>T MANE Select	NP_002326.2:p.Phe70=
NM_001291902.2:c.-1556C>T	NP_001278831.1:n.-1556C>T