Canonical Allele Identifier: CA631766641
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs1231756036

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113979_11113981del , CM000681.2:g.11113979_11113981del GRCh38
NC_000019.9:g.11224655_11224657del , CM000681.1:g.11224655_11224657del GRCh37
NC_000019.8:g.11085655_11085657del NCBI36
NG_009060.1:g.29599_29601del , LRG_274:g.29599_29601del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1844+217_1844+219del ENSP00000252444.6:n.1844+217_1844+219del
ENST00000559340.2:c.1586+217_1586+219del ENSP00000453696.2:n.1586+217_1586+219del
ENST00000560467.2:c.1466+217_1466+219del ENSP00000453513.2:n.1466+217_1466+219del
ENST00000558518.6:c.1586+217_1586+219del MANE Select ENSP00000454071.1:n.1586+217_1586+219del
ENST00000252444.9:c.1840+217_1840+219del
ENST00000455727.6:c.1082+217_1082+219del ENSP00000397829.2:n.1082+217_1082+219del
ENST00000535915.5:c.1463+217_1463+219del ENSP00000440520.1:n.1463+217_1463+219del
ENST00000545707.5:c.1205+217_1205+219del ENSP00000437639.1:n.1205+217_1205+219del
ENST00000557933.5:c.1586+217_1586+219del ENSP00000453557.1:n.1586+217_1586+219del
ENST00000558013.5:c.1586+217_1586+219del ENSP00000453346.1:n.1586+217_1586+219del
ENST00000558518.5:c.1586+217_1586+219del ENSP00000454071.1:n.1586+217_1586+219del
ENST00000559340.1:c.307+217_307+219del
NM_000527.4:c.1586+217_1586+219del , LRG_274t1:c.1586+217_1586+219del NP_000518.1:n.1586+217_1586+219del
NM_001195798.1:c.1586+217_1586+219del NP_001182727.1:n.1586+217_1586+219del
NM_001195799.1:c.1463+217_1463+219del NP_001182728.1:n.1463+217_1463+219del
NM_001195800.1:c.1082+217_1082+219del NP_001182729.1:n.1082+217_1082+219del
NM_001195803.1:c.1205+217_1205+219del NP_001182732.1:n.1205+217_1205+219del
XM_011528010.1:c.1586+217_1586+219del XP_011526312.1:n.1586+217_1586+219del
XM_011528011.1:c.1205+217_1205+219del XP_011526313.1:n.1205+217_1205+219del
XR_244074.2:n.1736+217_1736+219del
XM_011528010.2:c.1586+217_1586+219del XP_011526312.1:n.1586+217_1586+219del
XR_001753685.2:n.1703+217_1703+219del
XR_001753686.2:n.1703+217_1703+219del
NM_000527.5:c.1586+217_1586+219del MANE Select NP_000518.1:n.1586+217_1586+219del
NM_001195798.2:c.1586+217_1586+219del NP_001182727.1:n.1586+217_1586+219del
NM_001195799.2:c.1463+217_1463+219del NP_001182728.1:n.1463+217_1463+219del
NM_001195800.2:c.1082+217_1082+219del NP_001182729.1:n.1082+217_1082+219del
NM_001195803.2:c.1205+217_1205+219del NP_001182732.1:n.1205+217_1205+219del