Canonical Allele Identifier: CA339078739
Gene: LDLRAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25557235T>C , CM000663.2:g.25557235T>C GRCh38
NC_000001.10:g.25883726T>C , CM000663.1:g.25883726T>C GRCh37
NC_000001.9:g.25756313T>C NCBI36
NG_008932.1:g.18651T>C , LRG_276:g.18651T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.427T>C MANE Select ENSP00000363458.4:p.Cys143Arg
ENST00000374338.4:c.427T>C ENSP00000363458.4:p.Cys143Arg
ENST00000462394.1:n.175T>C
ENST00000488127.1:n.897T>C
NM_015627.2:c.427T>C , LRG_276t1:c.427T>C NP_056442.2:p.Cys143Arg
XM_006710559.2:c.427T>C XP_006710622.1:p.Cys143Arg
XM_006710560.2:c.427T>C XP_006710623.1:p.Cys143Arg
XM_006710561.2:c.427T>C XP_006710624.1:p.Cys143Arg
XM_011541209.1:c.427T>C XP_011539511.1:p.Cys143Arg
XM_011541210.1:c.427T>C XP_011539512.1:p.Cys143Arg
XM_011541211.1:c.427T>C XP_011539513.1:p.Cys143Arg
XM_011541212.1:c.427T>C XP_011539514.1:p.Cys143Arg
XR_426598.2:n.546T>C
XR_946602.1:n.546T>C
XR_946603.1:n.546T>C
XM_006710559.4:c.427T>C XP_006710622.1:p.Cys143Arg
XM_006710560.4:c.427T>C XP_006710623.1:p.Cys143Arg
XM_006710561.4:c.427T>C XP_006710624.1:p.Cys143Arg
XM_011541209.3:c.427T>C XP_011539511.1:p.Cys143Arg
XM_011541210.3:c.427T>C XP_011539512.1:p.Cys143Arg
XM_011541211.3:c.427T>C XP_011539513.1:p.Cys143Arg
XM_011541212.3:c.427T>C XP_011539514.1:p.Cys143Arg
XM_017000994.2:c.346T>C XP_016856483.1:p.Cys116Arg
XM_017000995.2:c.427T>C XP_016856484.1:p.Cys143Arg
XM_024446315.1:c.292T>C XP_024302083.1:p.Cys98Arg
XR_001737112.2:n.497T>C
XR_001737113.2:n.497T>C
XR_002956258.1:n.497T>C
XR_426598.4:n.497T>C
XR_946602.3:n.497T>C
XR_946603.3:n.497T>C
NM_015627.3:c.427T>C MANE Select NP_056442.2:p.Cys143Arg