Canonical Allele Identifier: CA505484937
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11217302C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11106626C>T , CM000681.2:g.11106626C>T GRCh38
NC_000019.9:g.11217302C>T , CM000681.1:g.11217302C>T GRCh37
NC_000019.8:g.11078302C>T NCBI36
NG_009060.1:g.22246C>T , LRG_274:g.22246C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1014C>T ENSP00000252444.6:p.Ser338=
ENST00000559340.2:c.756C>T ENSP00000453696.2:p.Ser252=
ENST00000560467.2:c.756C>T ENSP00000453513.2:p.Ser252=
ENST00000558518.6:c.756C>T MANE Select ENSP00000454071.1:p.Ser252=
ENST00000252444.9:c.1010C>T
ENST00000455727.6:c.314-766C>T ENSP00000397829.2:n.314-766C>T
ENST00000535915.5:c.633C>T ENSP00000440520.1:p.Ser211=
ENST00000545707.5:c.375C>T ENSP00000437639.1:p.Ser125=
ENST00000557933.5:c.756C>T ENSP00000453557.1:p.Ser252=
ENST00000558013.5:c.756C>T ENSP00000453346.1:p.Ser252=
ENST00000558518.5:c.756C>T ENSP00000454071.1:p.Ser252=
ENST00000558528.1:n.271C>T
ENST00000560467.1:c.356C>T
NM_000527.4:c.756C>T , LRG_274t1:c.756C>T NP_000518.1:p.Ser252=
NM_001195798.1:c.756C>T NP_001182727.1:p.Ser252=
NM_001195799.1:c.633C>T NP_001182728.1:p.Ser211=
NM_001195800.1:c.314-766C>T NP_001182729.1:n.314-766C>T
NM_001195803.1:c.375C>T NP_001182732.1:p.Ser125=
XM_011528010.1:c.756C>T XP_011526312.1:p.Ser252=
XM_011528011.1:c.375C>T XP_011526313.1:p.Ser125=
XR_244074.2:n.906C>T
XM_011528010.2:c.756C>T XP_011526312.1:p.Ser252=
XR_001753685.2:n.873C>T
XR_001753686.2:n.873C>T
NM_000527.5:c.756C>T MANE Select NP_000518.1:p.Ser252=
NM_001195798.2:c.756C>T NP_001182727.1:p.Ser252=
NM_001195799.2:c.633C>T NP_001182728.1:p.Ser211=
NM_001195800.2:c.314-766C>T NP_001182729.1:n.314-766C>T
NM_001195803.2:c.375C>T NP_001182732.1:p.Ser125=
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