Canonical Allele Identifier: CA404093887

Gene: LDLR

Linked Data

• gnomAD v4: 19-11120472-C-T
• MyVariant Identifiers: chr19:g.11231148C>T (hg19) ; chr19:g.11120472C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120472C>T , CM000681.2:g.11120472C>T	GRCh38
NC_000019.9:g.11231148C>T , CM000681.1:g.11231148C>T	GRCh37
NC_000019.8:g.11092148C>T	NCBI36
NG_009060.1:g.36092C>T , LRG_274:g.36092C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2348C>T	ENSP00000252444.6:p.Ala783Val
ENST00000559340.2:c.*159C>T	ENSP00000453696.2:n.*159C>T
ENST00000560467.2:c.1970C>T	ENSP00000453513.2:p.Ala657Val
ENST00000558518.6:c.2090C>T MANE Select	ENSP00000454071.1:p.Ala697Val
ENST00000252444.9:c.2344C>T
ENST00000455727.6:c.1586C>T	ENSP00000397829.2:p.Ala529Val
ENST00000535915.5:c.1967C>T	ENSP00000440520.1:p.Ala656Val
ENST00000545707.5:c.1606+239C>T	ENSP00000437639.1:n.1606+239C>T
ENST00000557933.5:c.2090C>T	ENSP00000453557.1:p.Ala697Val
ENST00000558013.5:c.2090C>T	ENSP00000453346.1:p.Ala697Val
ENST00000558518.5:c.2090C>T	ENSP00000454071.1:p.Ala697Val
NM_000527.4:c.2090C>T , LRG_274t1:c.2090C>T	NP_000518.1:p.Ala697Val
NM_001195798.1:c.2090C>T	NP_001182727.1:p.Ala697Val
NM_001195799.1:c.1967C>T	NP_001182728.1:p.Ala656Val
NM_001195800.1:c.1586C>T	NP_001182729.1:p.Ala529Val
NM_001195803.1:c.1606+239C>T	NP_001182732.1:n.1606+239C>T
XM_011528010.1:c.2090C>T	XP_011526312.1:p.Ala697Val
XM_011528011.1:c.1709C>T	XP_011526313.1:p.Ala570Val
XR_244074.2:n.2100C>T
XM_011528010.2:c.2090C>T	XP_011526312.1:p.Ala697Val
XR_001753685.2:n.2207C>T
XR_001753686.2:n.2067C>T
NM_000527.5:c.2090C>T MANE Select	NP_000518.1:p.Ala697Val
NM_001195798.2:c.2090C>T	NP_001182727.1:p.Ala697Val
NM_001195799.2:c.1967C>T	NP_001182728.1:p.Ala656Val
NM_001195800.2:c.1586C>T	NP_001182729.1:p.Ala529Val
NM_001195803.2:c.1606+239C>T	NP_001182732.1:n.1606+239C>T