Canonical Allele Identifier: CA339076668
Gene: LDLRAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25543758G>C , CM000663.2:g.25543758G>C GRCh38
NC_000001.10:g.25870249G>C , CM000663.1:g.25870249G>C GRCh37
NC_000001.9:g.25742836G>C NCBI36
NG_008932.1:g.5174G>C , LRG_276:g.5174G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.60G>C MANE Select ENSP00000363458.4:p.Gln20His
ENST00000374338.4:c.60G>C ENSP00000363458.4:p.Gln20His
NM_015627.2:c.60G>C , LRG_276t1:c.60G>C NP_056442.2:p.Gln20His
XM_006710559.2:c.60G>C XP_006710622.1:p.Gln20His
XM_006710560.2:c.60G>C XP_006710623.1:p.Gln20His
XM_006710561.2:c.60G>C XP_006710624.1:p.Gln20His
XM_011541209.1:c.60G>C XP_011539511.1:p.Gln20His
XM_011541210.1:c.60G>C XP_011539512.1:p.Gln20His
XM_011541211.1:c.60G>C XP_011539513.1:p.Gln20His
XM_011541212.1:c.60G>C XP_011539514.1:p.Gln20His
XR_426598.2:n.179G>C
XR_946602.1:n.179G>C
XR_946603.1:n.179G>C
XM_006710559.4:c.60G>C XP_006710622.1:p.Gln20His
XM_006710560.4:c.60G>C XP_006710623.1:p.Gln20His
XM_006710561.4:c.60G>C XP_006710624.1:p.Gln20His
XM_011541209.3:c.60G>C XP_011539511.1:p.Gln20His
XM_011541210.3:c.60G>C XP_011539512.1:p.Gln20His
XM_011541211.3:c.60G>C XP_011539513.1:p.Gln20His
XM_011541212.3:c.60G>C XP_011539514.1:p.Gln20His
XM_017000995.2:c.60G>C XP_016856484.1:p.Gln20His
XR_001737112.2:n.130G>C
XR_001737113.2:n.130G>C
XR_002956258.1:n.130G>C
XR_426598.4:n.130G>C
XR_946602.3:n.130G>C
XR_946603.3:n.130G>C
NM_015627.3:c.60G>C MANE Select NP_056442.2:p.Gln20His