Canonical Allele Identifier: CA404085395
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11224119T>G (hg19) chr19:g.11113443T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113443T>G , CM000681.2:g.11113443T>G GRCh38
NC_000019.9:g.11224119T>G , CM000681.1:g.11224119T>G GRCh37
NC_000019.8:g.11085119T>G NCBI36
NG_009060.1:g.29063T>G , LRG_274:g.29063T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1610T>G ENSP00000252444.6:p.Ile537Ser
ENST00000559340.2:c.1352T>G ENSP00000453696.2:p.Ile451Ser
ENST00000560467.2:c.1232T>G ENSP00000453513.2:p.Ile411Ser
ENST00000558518.6:c.1352T>G MANE Select ENSP00000454071.1:p.Ile451Ser
ENST00000252444.9:c.1606T>G
ENST00000455727.6:c.848T>G ENSP00000397829.2:p.Ile283Ser
ENST00000535915.5:c.1229T>G ENSP00000440520.1:p.Ile410Ser
ENST00000545707.5:c.971T>G ENSP00000437639.1:p.Ile324Ser
ENST00000557933.5:c.1352T>G ENSP00000453557.1:p.Ile451Ser
ENST00000558013.5:c.1352T>G ENSP00000453346.1:p.Ile451Ser
ENST00000558518.5:c.1352T>G ENSP00000454071.1:p.Ile451Ser
ENST00000559340.1:c.73T>G
ENST00000560173.1:n.351T>G
ENST00000560467.1:c.832T>G
NM_000527.4:c.1352T>G , LRG_274t1:c.1352T>G NP_000518.1:p.Ile451Ser
NM_001195798.1:c.1352T>G NP_001182727.1:p.Ile451Ser
NM_001195799.1:c.1229T>G NP_001182728.1:p.Ile410Ser
NM_001195800.1:c.848T>G NP_001182729.1:p.Ile283Ser
NM_001195803.1:c.971T>G NP_001182732.1:p.Ile324Ser
XM_011528010.1:c.1352T>G XP_011526312.1:p.Ile451Ser
XM_011528011.1:c.971T>G XP_011526313.1:p.Ile324Ser
XR_244074.2:n.1502T>G
XM_011528010.2:c.1352T>G XP_011526312.1:p.Ile451Ser
XR_001753685.2:n.1469T>G
XR_001753686.2:n.1469T>G
NM_000527.5:c.1352T>G MANE Select NP_000518.1:p.Ile451Ser
NM_001195798.2:c.1352T>G NP_001182727.1:p.Ile451Ser
NM_001195799.2:c.1229T>G NP_001182728.1:p.Ile410Ser
NM_001195800.2:c.848T>G NP_001182729.1:p.Ile283Ser
NM_001195803.2:c.971T>G NP_001182732.1:p.Ile324Ser
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