Canonical Allele Identifier: CA2735607973
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs2147229234

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11106687_11106688insTGACACTCT , CM000681.2:g.11106687_11106688insTGACACTCT GRCh38
NC_000019.9:g.11217363_11217364insTGACACTCT , CM000681.1:g.11217363_11217364insTGACACTCT GRCh37
NC_000019.8:g.11078363_11078364insTGACACTCT NCBI36
NG_009060.1:g.22307_22308insTGACACTCT , LRG_274:g.22307_22308insTGACACTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1075_1075+1insTGACACTCT ENSP00000252444.6:n.1075_1075+1insTGACACTCT
ENST00000559340.2:c.817_817+1insTGACACTCT ENSP00000453696.2:n.817_817+1insTGACACTCT
ENST00000560467.2:c.817_817+1insTGACACTCT ENSP00000453513.2:n.817_817+1insTGACACTCT
ENST00000558518.6:c.817_817+1insTGACACTCT MANE Select ENSP00000454071.1:n.817_817+1insTGACACTCT
ENST00000252444.9:c.1071_1071+1insTGACACTCT
ENST00000455727.6:c.314-705_314-704insTGACACTCT ENSP00000397829.2:n.314-705_314-704insTGACACTCT
ENST00000535915.5:c.694_694+1insTGACACTCT ENSP00000440520.1:n.694_694+1insTGACACTCT
ENST00000545707.5:c.436_436+1insTGACACTCT ENSP00000437639.1:n.436_436+1insTGACACTCT
ENST00000557933.5:c.817_817+1insTGACACTCT ENSP00000453557.1:n.817_817+1insTGACACTCT
ENST00000558013.5:c.817_817+1insTGACACTCT ENSP00000453346.1:n.817_817+1insTGACACTCT
ENST00000558518.5:c.817_817+1insTGACACTCT ENSP00000454071.1:n.817_817+1insTGACACTCT
ENST00000558528.1:n.332_332+1insTGACACTCT
ENST00000560467.1:c.417_417+1insTGACACTCT
NM_000527.4:c.817_817+1insTGACACTCT , LRG_274t1:c.817_817+1insTGACACTCT NP_000518.1:n.817_817+1insTGACACTCT
NM_001195798.1:c.817_817+1insTGACACTCT NP_001182727.1:n.817_817+1insTGACACTCT
NM_001195799.1:c.694_694+1insTGACACTCT NP_001182728.1:n.694_694+1insTGACACTCT
NM_001195800.1:c.314-705_314-704insTGACACTCT NP_001182729.1:n.314-705_314-704insTGACACTCT
NM_001195803.1:c.436_436+1insTGACACTCT NP_001182732.1:n.436_436+1insTGACACTCT
XM_011528010.1:c.817_817+1insTGACACTCT XP_011526312.1:n.817_817+1insTGACACTCT
XM_011528011.1:c.436_436+1insTGACACTCT XP_011526313.1:n.436_436+1insTGACACTCT
XR_244074.2:n.967_967+1insTGACACTCT
XM_011528010.2:c.817_817+1insTGACACTCT XP_011526312.1:n.817_817+1insTGACACTCT
XR_001753685.2:n.934_934+1insTGACACTCT
XR_001753686.2:n.934_934+1insTGACACTCT
NM_000527.5:c.817_817+1insTGACACTCT MANE Select NP_000518.1:n.817_817+1insTGACACTCT
NM_001195798.2:c.817_817+1insTGACACTCT NP_001182727.1:n.817_817+1insTGACACTCT
NM_001195799.2:c.694_694+1insTGACACTCT NP_001182728.1:n.694_694+1insTGACACTCT
NM_001195800.2:c.314-705_314-704insTGACACTCT NP_001182729.1:n.314-705_314-704insTGACACTCT
NM_001195803.2:c.436_436+1insTGACACTCT NP_001182732.1:n.436_436+1insTGACACTCT