Canonical Allele Identifier: CA404093840

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11231140T>A (hg19) ; chr19:g.11120464T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120464T>A , CM000681.2:g.11120464T>A	GRCh38
NC_000019.9:g.11231140T>A , CM000681.1:g.11231140T>A	GRCh37
NC_000019.8:g.11092140T>A	NCBI36
NG_009060.1:g.36084T>A , LRG_274:g.36084T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2340T>A	ENSP00000252444.6:p.Phe780Leu
ENST00000559340.2:c.*151T>A	ENSP00000453696.2:n.*151T>A
ENST00000560467.2:c.1962T>A	ENSP00000453513.2:p.Phe654Leu
ENST00000558518.6:c.2082T>A MANE Select	ENSP00000454071.1:p.Phe694Leu
ENST00000252444.9:c.2336T>A
ENST00000455727.6:c.1578T>A	ENSP00000397829.2:p.Phe526Leu
ENST00000535915.5:c.1959T>A	ENSP00000440520.1:p.Phe653Leu
ENST00000545707.5:c.1606+231T>A	ENSP00000437639.1:n.1606+231T>A
ENST00000557933.5:c.2082T>A	ENSP00000453557.1:p.Phe694Leu
ENST00000558013.5:c.2082T>A	ENSP00000453346.1:p.Phe694Leu
ENST00000558518.5:c.2082T>A	ENSP00000454071.1:p.Phe694Leu
NM_000527.4:c.2082T>A , LRG_274t1:c.2082T>A	NP_000518.1:p.Phe694Leu
NM_001195798.1:c.2082T>A	NP_001182727.1:p.Phe694Leu
NM_001195799.1:c.1959T>A	NP_001182728.1:p.Phe653Leu
NM_001195800.1:c.1578T>A	NP_001182729.1:p.Phe526Leu
NM_001195803.1:c.1606+231T>A	NP_001182732.1:n.1606+231T>A
XM_011528010.1:c.2082T>A	XP_011526312.1:p.Phe694Leu
XM_011528011.1:c.1701T>A	XP_011526313.1:p.Phe567Leu
XR_244074.2:n.2092T>A
XM_011528010.2:c.2082T>A	XP_011526312.1:p.Phe694Leu
XR_001753685.2:n.2199T>A
XR_001753686.2:n.2059T>A
NM_000527.5:c.2082T>A MANE Select	NP_000518.1:p.Phe694Leu
NM_001195798.2:c.2082T>A	NP_001182727.1:p.Phe694Leu
NM_001195799.2:c.1959T>A	NP_001182728.1:p.Phe653Leu
NM_001195800.2:c.1578T>A	NP_001182729.1:p.Phe526Leu
NM_001195803.2:c.1606+231T>A	NP_001182732.1:n.1606+231T>A