Canonical Allele Identifier: CA339078799
Gene: LDLRAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25557263A>C , CM000663.2:g.25557263A>C GRCh38
NC_000001.10:g.25883754A>C , CM000663.1:g.25883754A>C GRCh37
NC_000001.9:g.25756341A>C NCBI36
NG_008932.1:g.18679A>C , LRG_276:g.18679A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.455A>C MANE Select ENSP00000363458.4:p.Lys152Thr
ENST00000374338.4:c.455A>C ENSP00000363458.4:p.Lys152Thr
ENST00000462394.1:n.203A>C
ENST00000488127.1:n.925A>C
NM_015627.2:c.455A>C , LRG_276t1:c.455A>C NP_056442.2:p.Lys152Thr
XM_006710559.2:c.455A>C XP_006710622.1:p.Lys152Thr
XM_006710560.2:c.455A>C XP_006710623.1:p.Lys152Thr
XM_006710561.2:c.455A>C XP_006710624.1:p.Lys152Thr
XM_011541209.1:c.455A>C XP_011539511.1:p.Lys152Thr
XM_011541210.1:c.455A>C XP_011539512.1:p.Lys152Thr
XM_011541211.1:c.455A>C XP_011539513.1:p.Lys152Thr
XM_011541212.1:c.455A>C XP_011539514.1:p.Lys152Thr
XR_426598.2:n.574A>C
XR_946602.1:n.574A>C
XR_946603.1:n.574A>C
XM_006710559.4:c.455A>C XP_006710622.1:p.Lys152Thr
XM_006710560.4:c.455A>C XP_006710623.1:p.Lys152Thr
XM_006710561.4:c.455A>C XP_006710624.1:p.Lys152Thr
XM_011541209.3:c.455A>C XP_011539511.1:p.Lys152Thr
XM_011541210.3:c.455A>C XP_011539512.1:p.Lys152Thr
XM_011541211.3:c.455A>C XP_011539513.1:p.Lys152Thr
XM_011541212.3:c.455A>C XP_011539514.1:p.Lys152Thr
XM_017000994.2:c.374A>C XP_016856483.1:p.Lys125Thr
XM_017000995.2:c.455A>C XP_016856484.1:p.Lys152Thr
XM_024446315.1:c.320A>C XP_024302083.1:p.Lys107Thr
XR_001737112.2:n.525A>C
XR_001737113.2:n.525A>C
XR_002956258.1:n.525A>C
XR_426598.4:n.525A>C
XR_946602.3:n.525A>C
XR_946603.3:n.525A>C
NM_015627.3:c.455A>C MANE Select NP_056442.2:p.Lys152Thr