Canonical Allele Identifier: CA505743359

Gene: LDLR

Linked Data

• ClinVar Variation Id: 440668
• ClinVar RCV Id: RCV000508747 ; RCV002413395
• dbSNP Id: rs768509914
• MyVariant Identifiers: chr19:g.11230785A>C (hg19) ; chr19:g.11120109A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120109A>C , CM000681.2:g.11120109A>C	GRCh38
NC_000019.9:g.11230785A>C , CM000681.1:g.11230785A>C	GRCh37
NC_000019.8:g.11091785A>C	NCBI36
NG_009060.1:g.35729A>C , LRG_274:g.35729A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2121A>C	ENSP00000252444.6:p.Thr707=
ENST00000559340.2:c.1723A>C	ENSP00000453696.2:p.Arg575=
ENST00000560467.2:c.1743A>C	ENSP00000453513.2:p.Thr581=
ENST00000558518.6:c.1863A>C MANE Select	ENSP00000454071.1:p.Thr621=
ENST00000252444.9:c.2117A>C
ENST00000455727.6:c.1359A>C	ENSP00000397829.2:p.Thr453=
ENST00000535915.5:c.1740A>C	ENSP00000440520.1:p.Thr580=
ENST00000545707.5:c.1482A>C	ENSP00000437639.1:p.Thr494=
ENST00000557933.5:c.1863A>C	ENSP00000453557.1:p.Thr621=
ENST00000558013.5:c.1863A>C	ENSP00000453346.1:p.Thr621=
ENST00000558518.5:c.1863A>C	ENSP00000454071.1:p.Thr621=
ENST00000559340.1:c.444A>C
NM_000527.4:c.1863A>C , LRG_274t1:c.1863A>C	NP_000518.1:p.Thr621=
NM_001195798.1:c.1863A>C	NP_001182727.1:p.Thr621=
NM_001195799.1:c.1740A>C	NP_001182728.1:p.Thr580=
NM_001195800.1:c.1359A>C	NP_001182729.1:p.Thr453=
NM_001195803.1:c.1482A>C	NP_001182732.1:p.Thr494=
XM_011528010.1:c.1863A>C	XP_011526312.1:p.Thr621=
XM_011528011.1:c.1482A>C	XP_011526313.1:p.Thr494=
XR_244074.2:n.1873A>C
XM_011528010.2:c.1863A>C	XP_011526312.1:p.Thr621=
XR_001753685.2:n.1980A>C
XR_001753686.2:n.1840A>C
NM_000527.5:c.1863A>C MANE Select	NP_000518.1:p.Thr621=
NM_001195798.2:c.1863A>C	NP_001182727.1:p.Thr621=
NM_001195799.2:c.1740A>C	NP_001182728.1:p.Thr580=
NM_001195800.2:c.1359A>C	NP_001182729.1:p.Thr453=
NM_001195803.2:c.1482A>C	NP_001182732.1:p.Thr494=