Canonical Allele Identifier: CA2322771542
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113046_11113047delinsCT , CM000681.2:g.11113046_11113047delinsCT GRCh38
NC_000019.9:g.11223722_11223723delinsCT , CM000681.1:g.11223722_11223723delinsCT GRCh37
NC_000019.8:g.11084722_11084723delinsCT NCBI36
NG_009060.1:g.28666_28667delinsCT , LRG_274:g.28666_28667delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1445-232_1445-231delinsCT ENSP00000252444.6:n.1445-232_1445-231delinsCT
ENST00000559340.2:c.1187-232_1187-231delinsCT ENSP00000453696.2:n.1187-232_1187-231delinsCT
ENST00000560467.2:c.1067-232_1067-231delinsCT ENSP00000453513.2:n.1067-232_1067-231delinsCT
ENST00000558518.6:c.1187-232_1187-231delinsCT MANE Select ENSP00000454071.1:n.1187-232_1187-231delinsCT
ENST00000252444.9:c.1441-232_1441-231delinsCT
ENST00000455727.6:c.683-232_683-231delinsCT ENSP00000397829.2:n.683-232_683-231delinsCT
ENST00000535915.5:c.1064-232_1064-231delinsCT ENSP00000440520.1:n.1064-232_1064-231delinsCT
ENST00000545707.5:c.806-232_806-231delinsCT ENSP00000437639.1:n.806-232_806-231delinsCT
ENST00000557933.5:c.1187-232_1187-231delinsCT ENSP00000453557.1:n.1187-232_1187-231delinsCT
ENST00000558013.5:c.1187-232_1187-231delinsCT ENSP00000453346.1:n.1187-232_1187-231delinsCT
ENST00000558518.5:c.1187-232_1187-231delinsCT ENSP00000454071.1:n.1187-232_1187-231delinsCT
ENST00000560173.1:n.186-232_186-231delinsCT
ENST00000560467.1:c.667-232_667-231delinsCT
NM_000527.4:c.1187-232_1187-231delinsCT , LRG_274t1:c.1187-232_1187-231delinsCT NP_000518.1:n.1187-232_1187-231delinsCT
NM_001195798.1:c.1187-232_1187-231delinsCT NP_001182727.1:n.1187-232_1187-231delinsCT
NM_001195799.1:c.1064-232_1064-231delinsCT NP_001182728.1:n.1064-232_1064-231delinsCT
NM_001195800.1:c.683-232_683-231delinsCT NP_001182729.1:n.683-232_683-231delinsCT
NM_001195803.1:c.806-232_806-231delinsCT NP_001182732.1:n.806-232_806-231delinsCT
XM_011528010.1:c.1187-232_1187-231delinsCT XP_011526312.1:n.1187-232_1187-231delinsCT
XM_011528011.1:c.806-232_806-231delinsCT XP_011526313.1:n.806-232_806-231delinsCT
XR_244074.2:n.1337-232_1337-231delinsCT
XM_011528010.2:c.1187-232_1187-231delinsCT XP_011526312.1:n.1187-232_1187-231delinsCT
XR_001753685.2:n.1304-232_1304-231delinsCT
XR_001753686.2:n.1304-232_1304-231delinsCT
NM_000527.5:c.1187-232_1187-231delinsCT MANE Select NP_000518.1:n.1187-232_1187-231delinsCT
NM_001195798.2:c.1187-232_1187-231delinsCT NP_001182727.1:n.1187-232_1187-231delinsCT
NM_001195799.2:c.1064-232_1064-231delinsCT NP_001182728.1:n.1064-232_1064-231delinsCT
NM_001195800.2:c.683-232_683-231delinsCT NP_001182729.1:n.683-232_683-231delinsCT
NM_001195803.2:c.806-232_806-231delinsCT NP_001182732.1:n.806-232_806-231delinsCT