Canonical Allele Identifier: CA5969863
Community Standard Title: NM_002334.4(LRP4):c.2535A>C (p.Thr845=)
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46883948T>G , CM000673.2:g.46883948T>G GRCh38
NC_000011.9:g.46905499T>G , CM000673.1:g.46905499T>G GRCh37
NC_000011.8:g.46862075T>G NCBI36
NG_021394.1:g.39675A>C

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.2535A>C MANE Select NP_002325.2:p.Thr845=
ENST00000378623.6:c.2535A>C MANE Select ENSP00000367888.1:p.Thr845=
NM_002334.3:c.2535A>C NP_002325.2:p.Thr845=
ENST00000378623.5:c.2535A>C ENSP00000367888.1:p.Thr845=
ENST00000529921.1:n.566A>C
XM_011520102.1:c.2748A>C XP_011518404.1:p.Thr916=
XM_011520103.1:c.1731A>C XP_011518405.1:p.Thr577=
XM_011520103.2:c.1731A>C XP_011518405.1:p.Thr577=
XM_011520104.1:c.300A>C XP_011518406.1:p.Thr100=
XM_011520104.2:c.300A>C XP_011518406.1:p.Thr100=
XM_017017734.1:c.2535A>C XP_016873223.1:p.Thr845=