Canonical Allele Identifier: CA5969662
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46877220T>C , CM000673.2:g.46877220T>C GRCh38
NC_000011.9:g.46898771T>C , CM000673.1:g.46898771T>C GRCh37
NC_000011.8:g.46855347T>C NCBI36
NG_021394.1:g.46403A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378623.6:c.3256A>G MANE Select ENSP00000367888.1:p.Ile1086Val
ENST00000378623.5:c.3256A>G ENSP00000367888.1:p.Ile1086Val
NM_002334.3:c.3256A>G NP_002325.2:p.Ile1086Val
XM_011520102.1:c.3469A>G XP_011518404.1:p.Ile1157Val
XM_011520103.1:c.2452A>G XP_011518405.1:p.Ile818Val
XM_011520104.1:c.1021A>G XP_011518406.1:p.Ile341Val
XM_011520103.2:c.2452A>G XP_011518405.1:p.Ile818Val
XM_011520104.2:c.1021A>G XP_011518406.1:p.Ile341Val
XM_017017734.1:c.3256A>G XP_016873223.1:p.Ile1086Val
NM_002334.4:c.3256A>G MANE Select NP_002325.2:p.Ile1086Val