Canonical Allele Identifier: CA2322770259
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110706_11110720delinsTTAAGATCGGCTACG , CM000681.2:g.11110706_11110720delinsTTAAGATCGGCTACG GRCh38
NC_000019.9:g.11221382_11221396delinsTTAAGATCGGCTACG , CM000681.1:g.11221382_11221396delinsTTAAGATCGGCTACG GRCh37
NC_000019.8:g.11082382_11082396delinsTTAAGATCGGCTACG NCBI36
NG_009060.1:g.26326_26340delinsTTAAGATCGGCTACG , LRG_274:g.26326_26340delinsTTAAGATCGGCTACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1253_1267delinsTTAAGATCGGCTACG ENSP00000252444.6:p.Leu418=
ENST00000559340.2:c.995_1009delinsTTAAGATCGGCTACG ENSP00000453696.2:p.Leu332=
ENST00000560467.2:c.941-808_941-794delinsTTAAGATCGGCTACG ENSP00000453513.2:n.941-808_941-794delinsTTAAGATCGGCTACG
ENST00000558518.6:c.995_1009delinsTTAAGATCGGCTACG MANE Select ENSP00000454071.1:p.Leu332=
ENST00000252444.9:c.1249_1263delinsTTAAGATCGGCTACG
ENST00000455727.6:c.491_505delinsTTAAGATCGGCTACG ENSP00000397829.2:p.Leu164=
ENST00000535915.5:c.872_886delinsTTAAGATCGGCTACG ENSP00000440520.1:p.Leu291=
ENST00000545707.5:c.614_628delinsTTAAGATCGGCTACG ENSP00000437639.1:p.Leu205=
ENST00000557933.5:c.995_1009delinsTTAAGATCGGCTACG ENSP00000453557.1:p.Leu332=
ENST00000558013.5:c.995_1009delinsTTAAGATCGGCTACG ENSP00000453346.1:p.Leu332=
ENST00000558518.5:c.995_1009delinsTTAAGATCGGCTACG ENSP00000454071.1:p.Leu332=
ENST00000560467.1:c.541-808_541-794delinsTTAAGATCGGCTACG
NM_000527.4:c.995_1009delinsTTAAGATCGGCTACG , LRG_274t1:c.995_1009delinsTTAAGATCGGCTACG NP_000518.1:p.Leu332=
NM_001195798.1:c.995_1009delinsTTAAGATCGGCTACG NP_001182727.1:p.Leu332=
NM_001195799.1:c.872_886delinsTTAAGATCGGCTACG NP_001182728.1:p.Leu291=
NM_001195800.1:c.491_505delinsTTAAGATCGGCTACG NP_001182729.1:p.Leu164=
NM_001195803.1:c.614_628delinsTTAAGATCGGCTACG NP_001182732.1:p.Leu205=
XM_011528010.1:c.995_1009delinsTTAAGATCGGCTACG XP_011526312.1:p.Leu332=
XM_011528011.1:c.614_628delinsTTAAGATCGGCTACG XP_011526313.1:p.Leu205=
XR_244074.2:n.1145_1159delinsTTAAGATCGGCTACG
XM_011528010.2:c.995_1009delinsTTAAGATCGGCTACG XP_011526312.1:p.Leu332=
XR_001753685.2:n.1112_1126delinsTTAAGATCGGCTACG
XR_001753686.2:n.1112_1126delinsTTAAGATCGGCTACG
NM_000527.5:c.995_1009delinsTTAAGATCGGCTACG MANE Select NP_000518.1:p.Leu332=
NM_001195798.2:c.995_1009delinsTTAAGATCGGCTACG NP_001182727.1:p.Leu332=
NM_001195799.2:c.872_886delinsTTAAGATCGGCTACG NP_001182728.1:p.Leu291=
NM_001195800.2:c.491_505delinsTTAAGATCGGCTACG NP_001182729.1:p.Leu164=
NM_001195803.2:c.614_628delinsTTAAGATCGGCTACG NP_001182732.1:p.Leu205=