Canonical Allele Identifier: CA404093412
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120375A>C , CM000681.2:g.11120375A>C GRCh38
NC_000019.9:g.11231051A>C , CM000681.1:g.11231051A>C GRCh37
NC_000019.8:g.11092051A>C NCBI36
NG_009060.1:g.35995A>C , LRG_274:g.35995A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2251A>C ENSP00000252444.6:p.Asn751His
ENST00000559340.2:c.*62A>C ENSP00000453696.2:n.*62A>C
ENST00000560467.2:c.1873A>C ENSP00000453513.2:p.Asn625His
ENST00000558518.6:c.1993A>C MANE Select ENSP00000454071.1:p.Asn665His
ENST00000252444.9:c.2247A>C
ENST00000455727.6:c.1489A>C ENSP00000397829.2:p.Asn497His
ENST00000535915.5:c.1870A>C ENSP00000440520.1:p.Asn624His
ENST00000545707.5:c.1606+142A>C ENSP00000437639.1:n.1606+142A>C
ENST00000557933.5:c.1993A>C ENSP00000453557.1:p.Asn665His
ENST00000558013.5:c.1993A>C ENSP00000453346.1:p.Asn665His
ENST00000558518.5:c.1993A>C ENSP00000454071.1:p.Asn665His
ENST00000559340.1:c.574A>C
NM_000527.4:c.1993A>C , LRG_274t1:c.1993A>C NP_000518.1:p.Asn665His
NM_001195798.1:c.1993A>C NP_001182727.1:p.Asn665His
NM_001195799.1:c.1870A>C NP_001182728.1:p.Asn624His
NM_001195800.1:c.1489A>C NP_001182729.1:p.Asn497His
NM_001195803.1:c.1606+142A>C NP_001182732.1:n.1606+142A>C
XM_011528010.1:c.1993A>C XP_011526312.1:p.Asn665His
XM_011528011.1:c.1612A>C XP_011526313.1:p.Asn538His
XR_244074.2:n.2003A>C
XM_011528010.2:c.1993A>C XP_011526312.1:p.Asn665His
XR_001753685.2:n.2110A>C
XR_001753686.2:n.1970A>C
NM_000527.5:c.1993A>C MANE Select NP_000518.1:p.Asn665His
NM_001195798.2:c.1993A>C NP_001182727.1:p.Asn665His
NM_001195799.2:c.1870A>C NP_001182728.1:p.Asn624His
NM_001195800.2:c.1489A>C NP_001182729.1:p.Asn497His
NM_001195803.2:c.1606+142A>C NP_001182732.1:n.1606+142A>C