Canonical Allele Identifier: CA5969636
Community Standard Title: NM_002334.4(LRP4):c.3292T>A (p.Ser1098Thr)
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46876816A>T , CM000673.2:g.46876816A>T GRCh38
NC_000011.9:g.46898367A>T , CM000673.1:g.46898367A>T GRCh37
NC_000011.8:g.46854943A>T NCBI36
NG_021394.1:g.46807T>A

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3292T>A MANE Select NP_002325.2:p.Ser1098Thr
ENST00000378623.6:c.3292T>A MANE Select ENSP00000367888.1:p.Ser1098Thr
NM_002334.3:c.3292T>A NP_002325.2:p.Ser1098Thr
ENST00000378623.5:c.3292T>A ENSP00000367888.1:p.Ser1098Thr
XM_011520102.1:c.3505T>A XP_011518404.1:p.Ser1169Thr
XM_011520103.1:c.2488T>A XP_011518405.1:p.Ser830Thr
XM_011520103.2:c.2488T>A XP_011518405.1:p.Ser830Thr
XM_011520104.1:c.1057T>A XP_011518406.1:p.Ser353Thr
XM_011520104.2:c.1057T>A XP_011518406.1:p.Ser353Thr
XM_017017734.1:c.3292T>A XP_016873223.1:p.Ser1098Thr