Canonical Allele Identifier: CA404093536
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120403A>T , CM000681.2:g.11120403A>T GRCh38
NC_000019.9:g.11231079A>T , CM000681.1:g.11231079A>T GRCh37
NC_000019.8:g.11092079A>T NCBI36
NG_009060.1:g.36023A>T , LRG_274:g.36023A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.2279A>T ENSP00000252444.6:p.Asn760Ile
ENST00000559340.2:c.*90A>T ENSP00000453696.2:n.*90A>T
ENST00000560467.2:c.1901A>T ENSP00000453513.2:p.Asn634Ile
ENST00000558518.6:c.2021A>T MANE Select ENSP00000454071.1:p.Asn674Ile
ENST00000252444.9:c.2275A>T
ENST00000455727.6:c.1517A>T ENSP00000397829.2:p.Asn506Ile
ENST00000535915.5:c.1898A>T ENSP00000440520.1:p.Asn633Ile
ENST00000545707.5:c.1606+170A>T ENSP00000437639.1:n.1606+170A>T
ENST00000557933.5:c.2021A>T ENSP00000453557.1:p.Asn674Ile
ENST00000558013.5:c.2021A>T ENSP00000453346.1:p.Asn674Ile
ENST00000558518.5:c.2021A>T ENSP00000454071.1:p.Asn674Ile
ENST00000559340.1:c.602A>T
NM_000527.4:c.2021A>T , LRG_274t1:c.2021A>T NP_000518.1:p.Asn674Ile
NM_001195798.1:c.2021A>T NP_001182727.1:p.Asn674Ile
NM_001195799.1:c.1898A>T NP_001182728.1:p.Asn633Ile
NM_001195800.1:c.1517A>T NP_001182729.1:p.Asn506Ile
NM_001195803.1:c.1606+170A>T NP_001182732.1:n.1606+170A>T
XM_011528010.1:c.2021A>T XP_011526312.1:p.Asn674Ile
XM_011528011.1:c.1640A>T XP_011526313.1:p.Asn547Ile
XR_244074.2:n.2031A>T
XM_011528010.2:c.2021A>T XP_011526312.1:p.Asn674Ile
XR_001753685.2:n.2138A>T
XR_001753686.2:n.1998A>T
NM_000527.5:c.2021A>T MANE Select NP_000518.1:p.Asn674Ile
NM_001195798.2:c.2021A>T NP_001182727.1:p.Asn674Ile
NM_001195799.2:c.1898A>T NP_001182728.1:p.Asn633Ile
NM_001195800.2:c.1517A>T NP_001182729.1:p.Asn506Ile
NM_001195803.2:c.1606+170A>T NP_001182732.1:n.1606+170A>T