Canonical Allele Identifier: CA381614464

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68171086G>T (hg19) ; chr11:g.68403618G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68403618G>T , CM000673.2:g.68403618G>T	GRCh38
NC_000011.9:g.68171086G>T , CM000673.1:g.68171086G>T	GRCh37
NC_000011.8:g.67927662G>T	NCBI36
NG_015835.1:g.95979G>T
NG_015835.2:g.95979G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.1720G>T MANE Select	ENSP00000294304.6:p.Val574Phe
ENST00000294304.11:c.1720G>T	ENSP00000294304.6:p.Val574Phe
ENST00000529993.5:c.*132G>T	ENSP00000436652.1:n.*132G>T
NM_001291902.1:c.-218G>T	NP_001278831.1:n.-218G>T
NM_002335.3:c.1720G>T	NP_002326.2:p.Val574Phe
XM_005273994.2:c.1720G>T	XP_005274051.1:p.Val574Phe
XM_011545029.1:c.1747G>T	XP_011543331.1:p.Val583Phe
XM_011545030.1:c.1747G>T	XP_011543332.1:p.Val583Phe
XM_011545031.1:c.1747G>T	XP_011543333.1:p.Val583Phe
XR_949925.1:n.1762G>T
XR_949926.1:n.1762G>T
XR_001747874.1:n.1762G>T
XR_949925.2:n.1762G>T
XR_949926.2:n.1762G>T
NM_002335.4:c.1720G>T MANE Select	NP_002326.2:p.Val574Phe
NM_001291902.2:c.-218G>T	NP_001278831.1:n.-218G>T