Canonical Allele Identifier: CA505485060
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11218084A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107408A>C , CM000681.2:g.11107408A>C GRCh38
NC_000019.9:g.11218084A>C , CM000681.1:g.11218084A>C GRCh37
NC_000019.8:g.11079084A>C NCBI36
NG_009060.1:g.23028A>C , LRG_274:g.23028A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1092A>C ENSP00000252444.6:p.Gly364=
ENST00000559340.2:c.834A>C ENSP00000453696.2:p.Gly278=
ENST00000560467.2:c.834A>C ENSP00000453513.2:p.Gly278=
ENST00000558518.6:c.834A>C MANE Select ENSP00000454071.1:p.Gly278=
ENST00000252444.9:c.1088A>C
ENST00000455727.6:c.330A>C ENSP00000397829.2:p.Gly110=
ENST00000535915.5:c.711A>C ENSP00000440520.1:p.Gly237=
ENST00000545707.5:c.453A>C ENSP00000437639.1:p.Gly151=
ENST00000557933.5:c.834A>C ENSP00000453557.1:p.Gly278=
ENST00000558013.5:c.834A>C ENSP00000453346.1:p.Gly278=
ENST00000558518.5:c.834A>C ENSP00000454071.1:p.Gly278=
ENST00000558528.1:n.349A>C
ENST00000560467.1:c.434A>C
NM_000527.4:c.834A>C , LRG_274t1:c.834A>C NP_000518.1:p.Gly278=
NM_001195798.1:c.834A>C NP_001182727.1:p.Gly278=
NM_001195799.1:c.711A>C NP_001182728.1:p.Gly237=
NM_001195800.1:c.330A>C NP_001182729.1:p.Gly110=
NM_001195803.1:c.453A>C NP_001182732.1:p.Gly151=
XM_011528010.1:c.834A>C XP_011526312.1:p.Gly278=
XM_011528011.1:c.453A>C XP_011526313.1:p.Gly151=
XR_244074.2:n.984A>C
XM_011528010.2:c.834A>C XP_011526312.1:p.Gly278=
XR_001753685.2:n.951A>C
XR_001753686.2:n.951A>C
NM_000527.5:c.834A>C MANE Select NP_000518.1:p.Gly278=
NM_001195798.2:c.834A>C NP_001182727.1:p.Gly278=
NM_001195799.2:c.711A>C NP_001182728.1:p.Gly237=
NM_001195800.2:c.330A>C NP_001182729.1:p.Gly110=
NM_001195803.2:c.453A>C NP_001182732.1:p.Gly151=