Canonical Allele Identifier: CA1159701178
Gene: LDLRAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25543725G= , CM000663.2:g.25543725G= GRCh38
NC_000001.10:g.25870216G= , CM000663.1:g.25870216G= GRCh37
NC_000001.9:g.25742803G= NCBI36
NG_008932.1:g.5141G= , LRG_276:g.5141G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.27G= MANE Select ENSP00000363458.4:p.Arg9=
ENST00000374338.4:c.27G= ENSP00000363458.4:p.Arg9=
NM_015627.2:c.27G= , LRG_276t1:c.27G= NP_056442.2:p.Arg9=
XM_006710559.2:c.27G= XP_006710622.1:p.Arg9=
XM_006710560.2:c.27G= XP_006710623.1:p.Arg9=
XM_006710561.2:c.27G= XP_006710624.1:p.Arg9=
XM_011541209.1:c.27G= XP_011539511.1:p.Arg9=
XM_011541210.1:c.27G= XP_011539512.1:p.Arg9=
XM_011541211.1:c.27G= XP_011539513.1:p.Arg9=
XM_011541212.1:c.27G= XP_011539514.1:p.Arg9=
XR_426598.2:n.146G=
XR_946602.1:n.146G=
XR_946603.1:n.146G=
XM_006710559.4:c.27G= XP_006710622.1:p.Arg9=
XM_006710560.4:c.27G= XP_006710623.1:p.Arg9=
XM_006710561.4:c.27G= XP_006710624.1:p.Arg9=
XM_011541209.3:c.27G= XP_011539511.1:p.Arg9=
XM_011541210.3:c.27G= XP_011539512.1:p.Arg9=
XM_011541211.3:c.27G= XP_011539513.1:p.Arg9=
XM_011541212.3:c.27G= XP_011539514.1:p.Arg9=
XM_017000995.2:c.27G= XP_016856484.1:p.Arg9=
XR_001737112.2:n.97G=
XR_001737113.2:n.97G=
XR_002956258.1:n.97G=
XR_426598.4:n.97G=
XR_946602.3:n.97G=
XR_946603.3:n.97G=
NM_015627.3:c.27G= MANE Select NP_056442.2:p.Arg9=