Canonical Allele Identifier: CA695552
Gene: LDLRAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 296979
dbSNP Id: rs148916767
gnomAD v2: 1-25883750-C-T
gnomAD v3: 1-25557259-C-T
gnomAD v4: 1-25557259-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25557259C>T , CM000663.2:g.25557259C>T GRCh38
NC_000001.10:g.25883750C>T , CM000663.1:g.25883750C>T GRCh37
NC_000001.9:g.25756337C>T NCBI36
NG_008932.1:g.18675C>T , LRG_276:g.18675C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.451C>T MANE Select ENSP00000363458.4:p.Arg151Trp
ENST00000374338.4:c.451C>T ENSP00000363458.4:p.Arg151Trp
ENST00000462394.1:n.199C>T
ENST00000488127.1:n.921C>T
NM_015627.2:c.451C>T , LRG_276t1:c.451C>T NP_056442.2:p.Arg151Trp
XM_006710559.2:c.451C>T XP_006710622.1:p.Arg151Trp
XM_006710560.2:c.451C>T XP_006710623.1:p.Arg151Trp
XM_006710561.2:c.451C>T XP_006710624.1:p.Arg151Trp
XM_011541209.1:c.451C>T XP_011539511.1:p.Arg151Trp
XM_011541210.1:c.451C>T XP_011539512.1:p.Arg151Trp
XM_011541211.1:c.451C>T XP_011539513.1:p.Arg151Trp
XM_011541212.1:c.451C>T XP_011539514.1:p.Arg151Trp
XR_426598.2:n.570C>T
XR_946602.1:n.570C>T
XR_946603.1:n.570C>T
XM_006710559.4:c.451C>T XP_006710622.1:p.Arg151Trp
XM_006710560.4:c.451C>T XP_006710623.1:p.Arg151Trp
XM_006710561.4:c.451C>T XP_006710624.1:p.Arg151Trp
XM_011541209.3:c.451C>T XP_011539511.1:p.Arg151Trp
XM_011541210.3:c.451C>T XP_011539512.1:p.Arg151Trp
XM_011541211.3:c.451C>T XP_011539513.1:p.Arg151Trp
XM_011541212.3:c.451C>T XP_011539514.1:p.Arg151Trp
XM_017000994.2:c.370C>T XP_016856483.1:p.Arg124Trp
XM_017000995.2:c.451C>T XP_016856484.1:p.Arg151Trp
XM_024446315.1:c.316C>T XP_024302083.1:p.Arg106Trp
XR_001737112.2:n.521C>T
XR_001737113.2:n.521C>T
XR_002956258.1:n.521C>T
XR_426598.4:n.521C>T
XR_946602.3:n.521C>T
XR_946603.3:n.521C>T
NM_015627.3:c.451C>T MANE Select NP_056442.2:p.Arg151Trp