Canonical Allele Identifier: CA505743499
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs1428370694

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120431T>C , CM000681.2:g.11120431T>C GRCh38
NC_000019.9:g.11231107T>C , CM000681.1:g.11231107T>C GRCh37
NC_000019.8:g.11092107T>C NCBI36
NG_009060.1:g.36051T>C , LRG_274:g.36051T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2307T>C ENSP00000252444.6:p.Pro769=
ENST00000559340.2:c.*118T>C ENSP00000453696.2:n.*118T>C
ENST00000560467.2:c.1929T>C ENSP00000453513.2:p.Pro643=
ENST00000558518.6:c.2049T>C MANE Select ENSP00000454071.1:p.Pro683=
ENST00000252444.9:c.2303T>C
ENST00000455727.6:c.1545T>C ENSP00000397829.2:p.Pro515=
ENST00000535915.5:c.1926T>C ENSP00000440520.1:p.Pro642=
ENST00000545707.5:c.1606+198T>C ENSP00000437639.1:n.1606+198T>C
ENST00000557933.5:c.2049T>C ENSP00000453557.1:p.Pro683=
ENST00000558013.5:c.2049T>C ENSP00000453346.1:p.Pro683=
ENST00000558518.5:c.2049T>C ENSP00000454071.1:p.Pro683=
NM_000527.4:c.2049T>C , LRG_274t1:c.2049T>C NP_000518.1:p.Pro683=
NM_001195798.1:c.2049T>C NP_001182727.1:p.Pro683=
NM_001195799.1:c.1926T>C NP_001182728.1:p.Pro642=
NM_001195800.1:c.1545T>C NP_001182729.1:p.Pro515=
NM_001195803.1:c.1606+198T>C NP_001182732.1:n.1606+198T>C
XM_011528010.1:c.2049T>C XP_011526312.1:p.Pro683=
XM_011528011.1:c.1668T>C XP_011526313.1:p.Pro556=
XR_244074.2:n.2059T>C
XM_011528010.2:c.2049T>C XP_011526312.1:p.Pro683=
XR_001753685.2:n.2166T>C
XR_001753686.2:n.2026T>C
NM_000527.5:c.2049T>C MANE Select NP_000518.1:p.Pro683=
NM_001195798.2:c.2049T>C NP_001182727.1:p.Pro683=
NM_001195799.2:c.1926T>C NP_001182728.1:p.Pro642=
NM_001195800.2:c.1545T>C NP_001182729.1:p.Pro515=
NM_001195803.2:c.1606+198T>C NP_001182732.1:n.1606+198T>C