Canonical Allele Identifier: CA2322775529
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120375_11120392delinsAACTGGTGTGAGAGGACC , CM000681.2:g.11120375_11120392delinsAACTGGTGTGAGAGGACC GRCh38
NC_000019.9:g.11231051_11231068delinsAACTGGTGTGAGAGGACC , CM000681.1:g.11231051_11231068delinsAACTGGTGTGAGAGGACC GRCh37
NC_000019.8:g.11092051_11092068delinsAACTGGTGTGAGAGGACC NCBI36
NG_009060.1:g.35995_36012delinsAACTGGTGTGAGAGGACC , LRG_274:g.35995_36012delinsAACTGGTGTGAGAGGACC

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.2251_2268delinsAACTGGTGTGAGAGGACC ENSP00000252444.6:p.Asn751=
ENST00000559340.2:c.*62_*79delinsAACTGGTGTGAGAGGACC ENSP00000453696.2:n.*62_*79delinsAACTGGTG...
ENST00000560467.2:c.1873_1890delinsAACTGGTGTGAGAGGACC ENSP00000453513.2:p.Asn625=
ENST00000558518.6:c.1993_2010delinsAACTGGTGTGAGAGGACC MANE Select ENSP00000454071.1:p.Asn665=
ENST00000252444.9:c.2247_2264delinsAACTGGTGTGAGAGGACC
ENST00000455727.6:c.1489_1506delinsAACTGGTGTGAGAGGACC ENSP00000397829.2:p.Asn497=
ENST00000535915.5:c.1870_1887delinsAACTGGTGTGAGAGGACC ENSP00000440520.1:p.Asn624=
ENST00000545707.5:c.1606+142_1606+159delinsAACTGGTGTGAGAGGACC ENSP00000437639.1:n.1606+142_1606+159deli...
ENST00000557933.5:c.1993_2010delinsAACTGGTGTGAGAGGACC ENSP00000453557.1:p.Asn665=
ENST00000558013.5:c.1993_2010delinsAACTGGTGTGAGAGGACC ENSP00000453346.1:p.Asn665=
ENST00000558518.5:c.1993_2010delinsAACTGGTGTGAGAGGACC ENSP00000454071.1:p.Asn665=
ENST00000559340.1:c.574_591delinsAACTGGTGTGAGAGGACC
NM_000527.4:c.1993_2010delinsAACTGGTGTGAGAGGACC , LRG_274t1:c.1993_2010delinsAACTGGTGTGAGAGGACC NP_000518.1:p.Asn665=
NM_001195798.1:c.1993_2010delinsAACTGGTGTGAGAGGACC NP_001182727.1:p.Asn665=
NM_001195799.1:c.1870_1887delinsAACTGGTGTGAGAGGACC NP_001182728.1:p.Asn624=
NM_001195800.1:c.1489_1506delinsAACTGGTGTGAGAGGACC NP_001182729.1:p.Asn497=
NM_001195803.1:c.1606+142_1606+159delinsAACTGGTGTGAGAGGACC NP_001182732.1:n.1606+142_1606+159delinsA...
XM_011528010.1:c.1993_2010delinsAACTGGTGTGAGAGGACC XP_011526312.1:p.Asn665=
XM_011528011.1:c.1612_1629delinsAACTGGTGTGAGAGGACC XP_011526313.1:p.Asn538=
XR_244074.2:n.2003_2020delinsAACTGGTGTGAGAGGACC
XM_011528010.2:c.1993_2010delinsAACTGGTGTGAGAGGACC XP_011526312.1:p.Asn665=
XR_001753685.2:n.2110_2127delinsAACTGGTGTGAGAGGACC
XR_001753686.2:n.1970_1987delinsAACTGGTGTGAGAGGACC
NM_000527.5:c.1993_2010delinsAACTGGTGTGAGAGGACC MANE Select NP_000518.1:p.Asn665=
NM_001195798.2:c.1993_2010delinsAACTGGTGTGAGAGGACC NP_001182727.1:p.Asn665=
NM_001195799.2:c.1870_1887delinsAACTGGTGTGAGAGGACC NP_001182728.1:p.Asn624=
NM_001195800.2:c.1489_1506delinsAACTGGTGTGAGAGGACC NP_001182729.1:p.Asn497=
NM_001195803.2:c.1606+142_1606+159delinsAACTGGTGTGAGAGGACC NP_001182732.1:n.1606+142_1606+159delinsA...