Canonical Allele Identifier: CA5969597
Community Standard Title: NM_002334.4(LRP4):c.3429G>A (p.Thr1143=)
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46876573C>T , CM000673.2:g.46876573C>T GRCh38
NC_000011.9:g.46898124C>T , CM000673.1:g.46898124C>T GRCh37
NC_000011.8:g.46854700C>T NCBI36
NG_021394.1:g.47050G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3429G>A MANE Select NP_002325.2:p.Thr1143=
ENST00000378623.6:c.3429G>A MANE Select ENSP00000367888.1:p.Thr1143=
NM_002334.3:c.3429G>A NP_002325.2:p.Thr1143=
ENST00000378623.5:c.3429G>A ENSP00000367888.1:p.Thr1143=
XM_011520102.1:c.3642G>A XP_011518404.1:p.Thr1214=
XM_011520103.1:c.2625G>A XP_011518405.1:p.Thr875=
XM_011520103.2:c.2625G>A XP_011518405.1:p.Thr875=
XM_011520104.1:c.1194G>A XP_011518406.1:p.Thr398=
XM_011520104.2:c.1194G>A XP_011518406.1:p.Thr398=
XM_017017734.1:c.3429G>A XP_016873223.1:p.Thr1143=