Canonical Allele Identifier: CA2837994633
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107418_11107426delinsGGACTTCAAG , CM000681.2:g.11107418_11107426delinsGGACTTCAAG GRCh38
NC_000019.9:g.11218094_11218102delinsGGACTTCAAG , CM000681.1:g.11218094_11218102delinsGGACTTCAAG GRCh37
NC_000019.8:g.11079094_11079102delinsGGACTTCAAG NCBI36
NG_009060.1:g.23038_23046delinsGGACTTCAAG , LRG_274:g.23038_23046delinsGGACTTCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1102_1110delinsGGACTTCAAG ENSP00000252444.6:p.Phe368GlyfsTer19
ENST00000559340.2:c.844_852delinsGGACTTCAAG ENSP00000453696.2:p.Phe282GlyfsTer19
ENST00000560467.2:c.844_852delinsGGACTTCAAG ENSP00000453513.2:p.Phe282GlyfsTer19
ENST00000558518.6:c.844_852delinsGGACTTCAAG MANE Select ENSP00000454071.1:p.Phe282GlyfsTer19
ENST00000252444.9:c.1098_1106delinsGGACTTCAAG
ENST00000455727.6:c.340_348delinsGGACTTCAAG ENSP00000397829.2:p.Phe114GlyfsTer19
ENST00000535915.5:c.721_729delinsGGACTTCAAG ENSP00000440520.1:p.Phe241GlyfsTer19
ENST00000545707.5:c.463_471delinsGGACTTCAAG ENSP00000437639.1:p.Phe155GlyfsTer19
ENST00000557933.5:c.844_852delinsGGACTTCAAG ENSP00000453557.1:p.Phe282GlyfsTer19
ENST00000558013.5:c.844_852delinsGGACTTCAAG ENSP00000453346.1:p.Phe282GlyfsTer19
ENST00000558518.5:c.844_852delinsGGACTTCAAG ENSP00000454071.1:p.Phe282GlyfsTer19
ENST00000558528.1:n.359_367delinsGGACTTCAAG
ENST00000560467.1:c.444_452delinsGGACTTCAAG
NM_000527.4:c.844_852delinsGGACTTCAAG , LRG_274t1:c.844_852delinsGGACTTCAAG NP_000518.1:p.Phe282GlyfsTer19
NM_001195798.1:c.844_852delinsGGACTTCAAG NP_001182727.1:p.Phe282GlyfsTer19
NM_001195799.1:c.721_729delinsGGACTTCAAG NP_001182728.1:p.Phe241GlyfsTer19
NM_001195800.1:c.340_348delinsGGACTTCAAG NP_001182729.1:p.Phe114GlyfsTer19
NM_001195803.1:c.463_471delinsGGACTTCAAG NP_001182732.1:p.Phe155GlyfsTer19
XM_011528010.1:c.844_852delinsGGACTTCAAG XP_011526312.1:p.Phe282GlyfsTer19
XM_011528011.1:c.463_471delinsGGACTTCAAG XP_011526313.1:p.Phe155GlyfsTer19
XR_244074.2:n.994_1002delinsGGACTTCAAG
XM_011528010.2:c.844_852delinsGGACTTCAAG XP_011526312.1:p.Phe282GlyfsTer19
XR_001753685.2:n.961_969delinsGGACTTCAAG
XR_001753686.2:n.961_969delinsGGACTTCAAG
NM_000527.5:c.844_852delinsGGACTTCAAG MANE Select NP_000518.1:p.Phe282GlyfsTer19
NM_001195798.2:c.844_852delinsGGACTTCAAG NP_001182727.1:p.Phe282GlyfsTer19
NM_001195799.2:c.721_729delinsGGACTTCAAG NP_001182728.1:p.Phe241GlyfsTer19
NM_001195800.2:c.340_348delinsGGACTTCAAG NP_001182729.1:p.Phe114GlyfsTer19
NM_001195803.2:c.463_471delinsGGACTTCAAG NP_001182732.1:p.Phe155GlyfsTer19