Canonical Allele Identifier: CA2322780326
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129657_11129660delinsACAG , CM000681.2:g.11129657_11129660delinsACAG GRCh38
NC_000019.9:g.11240333_11240336delinsACAG , CM000681.1:g.11240333_11240336delinsACAG GRCh37
NC_000019.8:g.11101333_11101336delinsACAG NCBI36
NG_009060.1:g.45277_45280delinsACAG , LRG_274:g.45277_45280delinsACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2792_2795delinsACAG ENSP00000252444.6:p.Tyr931=
ENST00000559340.2:c.*603_*606delinsACAG ENSP00000453696.2:n.*603_*606delinsACAG
ENST00000560467.2:c.2414_2417delinsACAG ENSP00000453513.2:p.Tyr805=
ENST00000558518.6:c.2534_2537delinsACAG MANE Select ENSP00000454071.1:p.Tyr845=
ENST00000252444.9:c.2788_2791delinsACAG
ENST00000455727.6:c.2030_2033delinsACAG ENSP00000397829.2:p.Tyr677=
ENST00000535915.5:c.2411_2414delinsACAG ENSP00000440520.1:p.Tyr804=
ENST00000545707.5:c.2000_2003delinsACAG ENSP00000437639.1:p.Tyr667=
ENST00000557933.5:c.2596_2599delinsACAG ENSP00000453557.1:p.Thr866=
ENST00000558013.5:c.2534_2537delinsACAG ENSP00000453346.1:p.Tyr845=
ENST00000558518.5:c.2534_2537delinsACAG ENSP00000454071.1:p.Tyr845=
ENST00000560628.1:n.108+2003_108+2006delinsACAG
NM_000527.4:c.2534_2537delinsACAG , LRG_274t1:c.2534_2537delinsACAG NP_000518.1:p.Tyr845=
NM_001195798.1:c.2534_2537delinsACAG NP_001182727.1:p.Tyr845=
NM_001195799.1:c.2411_2414delinsACAG NP_001182728.1:p.Tyr804=
NM_001195800.1:c.2030_2033delinsACAG NP_001182729.1:p.Tyr677=
NM_001195803.1:c.2000_2003delinsACAG NP_001182732.1:p.Tyr667=
XM_011528010.1:c.2456_2459delinsACAG XP_011526312.1:p.Tyr819=
XM_011528011.1:c.2153_2156delinsACAG XP_011526313.1:p.Tyr718=
XM_011528010.2:c.2456_2459delinsACAG XP_011526312.1:p.Tyr819=
XR_001753685.2:n.2868_2871delinsACAG
XR_001753686.2:n.2511_2514delinsACAG
NM_000527.5:c.2534_2537delinsACAG MANE Select NP_000518.1:p.Tyr845=
NM_001195798.2:c.2534_2537delinsACAG NP_001182727.1:p.Tyr845=
NM_001195799.2:c.2411_2414delinsACAG NP_001182728.1:p.Tyr804=
NM_001195800.2:c.2030_2033delinsACAG NP_001182729.1:p.Tyr677=
NM_001195803.2:c.2000_2003delinsACAG NP_001182732.1:p.Tyr667=