Canonical Allele Identifier: CA10585228
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251573
dbSNP Id: rs879254740

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110672_11110673del , CM000681.2:g.11110672_11110673del GRCh38
NC_000019.9:g.11221348_11221349del , CM000681.1:g.11221348_11221349del GRCh37
NC_000019.8:g.11082348_11082349del NCBI36
NG_009060.1:g.26292_26293del , LRG_274:g.26292_26293del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1219_1220del ENSP00000252444.6:p.Asn407GlnfsTer10
ENST00000559340.2:c.961_962del ENSP00000453696.2:p.Asn321GlnfsTer10
ENST00000560467.2:c.941-842_941-841del ENSP00000453513.2:n.941-842_941-841del
ENST00000558518.6:c.961_962del MANE Select ENSP00000454071.1:p.Asn321GlnfsTer10
ENST00000252444.9:c.1215_1216del
ENST00000455727.6:c.457_458del ENSP00000397829.2:p.Asn153GlnfsTer10
ENST00000535915.5:c.838_839del ENSP00000440520.1:p.Asn280GlnfsTer10
ENST00000545707.5:c.580_581del ENSP00000437639.1:p.Asn194GlnfsTer10
ENST00000557933.5:c.961_962del ENSP00000453557.1:p.Asn321GlnfsTer10
ENST00000558013.5:c.961_962del ENSP00000453346.1:p.Asn321GlnfsTer10
ENST00000558518.5:c.961_962del ENSP00000454071.1:p.Asn321GlnfsTer10
ENST00000560467.1:c.541-842_541-841del
NM_000527.4:c.961_962del , LRG_274t1:c.961_962del NP_000518.1:p.Asn321GlnfsTer10
NM_001195798.1:c.961_962del NP_001182727.1:p.Asn321GlnfsTer10
NM_001195799.1:c.838_839del NP_001182728.1:p.Asn280GlnfsTer10
NM_001195800.1:c.457_458del NP_001182729.1:p.Asn153GlnfsTer10
NM_001195803.1:c.580_581del NP_001182732.1:p.Asn194GlnfsTer10
XM_011528010.1:c.961_962del XP_011526312.1:p.Asn321GlnfsTer10
XM_011528011.1:c.580_581del XP_011526313.1:p.Asn194GlnfsTer10
XR_244074.2:n.1111_1112del
XM_011528010.2:c.961_962del XP_011526312.1:p.Asn321GlnfsTer10
XR_001753685.2:n.1078_1079del
XR_001753686.2:n.1078_1079del
NM_000527.5:c.961_962del MANE Select NP_000518.1:p.Asn321GlnfsTer10
NM_001195798.2:c.961_962del NP_001182727.1:p.Asn321GlnfsTer10
NM_001195799.2:c.838_839del NP_001182728.1:p.Asn280GlnfsTer10
NM_001195800.2:c.457_458del NP_001182729.1:p.Asn153GlnfsTer10
NM_001195803.2:c.580_581del NP_001182732.1:p.Asn194GlnfsTer10