Canonical Allele Identifier: CA404080816

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11218118A>T (hg19) ; chr19:g.11107442A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107442A>T , CM000681.2:g.11107442A>T	GRCh38
NC_000019.9:g.11218118A>T , CM000681.1:g.11218118A>T	GRCh37
NC_000019.8:g.11079118A>T	NCBI36
NG_009060.1:g.23062A>T , LRG_274:g.23062A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1126A>T	ENSP00000252444.6:p.Ile376Phe
ENST00000559340.2:c.868A>T	ENSP00000453696.2:p.Ile290Phe
ENST00000560467.2:c.868A>T	ENSP00000453513.2:p.Ile290Phe
ENST00000558518.6:c.868A>T MANE Select	ENSP00000454071.1:p.Ile290Phe
ENST00000252444.9:c.1122A>T
ENST00000455727.6:c.364A>T	ENSP00000397829.2:p.Ile122Phe
ENST00000535915.5:c.745A>T	ENSP00000440520.1:p.Ile249Phe
ENST00000545707.5:c.487A>T	ENSP00000437639.1:p.Ile163Phe
ENST00000557933.5:c.868A>T	ENSP00000453557.1:p.Ile290Phe
ENST00000558013.5:c.868A>T	ENSP00000453346.1:p.Ile290Phe
ENST00000558518.5:c.868A>T	ENSP00000454071.1:p.Ile290Phe
ENST00000558528.1:n.383A>T
ENST00000560467.1:c.468A>T
NM_000527.4:c.868A>T , LRG_274t1:c.868A>T	NP_000518.1:p.Ile290Phe
NM_001195798.1:c.868A>T	NP_001182727.1:p.Ile290Phe
NM_001195799.1:c.745A>T	NP_001182728.1:p.Ile249Phe
NM_001195800.1:c.364A>T	NP_001182729.1:p.Ile122Phe
NM_001195803.1:c.487A>T	NP_001182732.1:p.Ile163Phe
XM_011528010.1:c.868A>T	XP_011526312.1:p.Ile290Phe
XM_011528011.1:c.487A>T	XP_011526313.1:p.Ile163Phe
XR_244074.2:n.1018A>T
XM_011528010.2:c.868A>T	XP_011526312.1:p.Ile290Phe
XR_001753685.2:n.985A>T
XR_001753686.2:n.985A>T
NM_000527.5:c.868A>T MANE Select	NP_000518.1:p.Ile290Phe
NM_001195798.2:c.868A>T	NP_001182727.1:p.Ile290Phe
NM_001195799.2:c.745A>T	NP_001182728.1:p.Ile249Phe
NM_001195800.2:c.364A>T	NP_001182729.1:p.Ile122Phe
NM_001195803.2:c.487A>T	NP_001182732.1:p.Ile163Phe