Canonical Allele Identifier: CA2322780247
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129519_11129535delinsTCGTCTTCCTTTGCCTG , CM000681.2:g.11129519_11129535delinsTCGTCTTCCTTTGCCTG GRCh38
NC_000019.9:g.11240195_11240211delinsTCGTCTTCCTTTGCCTG , CM000681.1:g.11240195_11240211delinsTCGTCTTCCTTTGCCTG GRCh37
NC_000019.8:g.11101195_11101211delinsTCGTCTTCCTTTGCCTG NCBI36
NG_009060.1:g.45139_45155delinsTCGTCTTCCTTTGCCTG , LRG_274:g.45139_45155delinsTCGTCTTCCTTTGCCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.2654_2670delinsTCGTCTTCCTTTGCCTG ENSP00000252444.6:p.Leu885=
ENST00000559340.2:c.*465_*481delinsTCGTCTTCCTTTGCCTG ENSP00000453696.2:n.*465_*481delinsTCGTCT...
ENST00000560467.2:c.2276_2292delinsTCGTCTTCCTTTGCCTG ENSP00000453513.2:p.Leu759=
ENST00000558518.6:c.2396_2412delinsTCGTCTTCCTTTGCCTG MANE Select ENSP00000454071.1:p.Leu799=
ENST00000252444.9:c.2650_2666delinsTCGTCTTCCTTTGCCTG
ENST00000455727.6:c.1892_1908delinsTCGTCTTCCTTTGCCTG ENSP00000397829.2:p.Leu631=
ENST00000535915.5:c.2273_2289delinsTCGTCTTCCTTTGCCTG ENSP00000440520.1:p.Leu758=
ENST00000545707.5:c.1862_1878delinsTCGTCTTCCTTTGCCTG ENSP00000437639.1:p.Leu621=
ENST00000557933.5:c.2458_2474delinsTCGTCTTCCTTTGCCTG ENSP00000453557.1:p.Ser820=
ENST00000558013.5:c.2396_2412delinsTCGTCTTCCTTTGCCTG ENSP00000453346.1:p.Leu799=
ENST00000558518.5:c.2396_2412delinsTCGTCTTCCTTTGCCTG ENSP00000454071.1:p.Leu799=
ENST00000560628.1:n.108+1865_108+1881delinsTCGTCTTCCTTTGCCTG
NM_000527.4:c.2396_2412delinsTCGTCTTCCTTTGCCTG , LRG_274t1:c.2396_2412delinsTCGTCTTCCTTTGCCTG NP_000518.1:p.Leu799=
NM_001195798.1:c.2396_2412delinsTCGTCTTCCTTTGCCTG NP_001182727.1:p.Leu799=
NM_001195799.1:c.2273_2289delinsTCGTCTTCCTTTGCCTG NP_001182728.1:p.Leu758=
NM_001195800.1:c.1892_1908delinsTCGTCTTCCTTTGCCTG NP_001182729.1:p.Leu631=
NM_001195803.1:c.1862_1878delinsTCGTCTTCCTTTGCCTG NP_001182732.1:p.Leu621=
XM_011528010.1:c.2318_2334delinsTCGTCTTCCTTTGCCTG XP_011526312.1:p.Leu773=
XM_011528011.1:c.2015_2031delinsTCGTCTTCCTTTGCCTG XP_011526313.1:p.Leu672=
XR_244074.2:n.2406_2422delinsTCGTCTTCCTTTGCCTG
XM_011528010.2:c.2318_2334delinsTCGTCTTCCTTTGCCTG XP_011526312.1:p.Leu773=
XR_001753685.2:n.2730_2746delinsTCGTCTTCCTTTGCCTG
XR_001753686.2:n.2373_2389delinsTCGTCTTCCTTTGCCTG
NM_000527.5:c.2396_2412delinsTCGTCTTCCTTTGCCTG MANE Select NP_000518.1:p.Leu799=
NM_001195798.2:c.2396_2412delinsTCGTCTTCCTTTGCCTG NP_001182727.1:p.Leu799=
NM_001195799.2:c.2273_2289delinsTCGTCTTCCTTTGCCTG NP_001182728.1:p.Leu758=
NM_001195800.2:c.1892_1908delinsTCGTCTTCCTTTGCCTG NP_001182729.1:p.Leu631=
NM_001195803.2:c.1862_1878delinsTCGTCTTCCTTTGCCTG NP_001182732.1:p.Leu621=