Canonical Allele Identifier: CA404084724

Gene: LDLR

Linked Data

• ClinVar Variation Id: 841257
• ClinVar RCV Id: RCV001043440
• dbSNP Id: rs2077408020
• gnomAD v4: 19-11113319-A-G
• MyVariant Identifiers: chr19:g.11223995A>G (hg19) ; chr19:g.11113319A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113319A>G , CM000681.2:g.11113319A>G	GRCh38
NC_000019.9:g.11223995A>G , CM000681.1:g.11223995A>G	GRCh37
NC_000019.8:g.11084995A>G	NCBI36
NG_009060.1:g.28939A>G , LRG_274:g.28939A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1486A>G	ENSP00000252444.6:p.Arg496Gly
ENST00000559340.2:c.1228A>G	ENSP00000453696.2:p.Arg410Gly
ENST00000560467.2:c.1108A>G	ENSP00000453513.2:p.Arg370Gly
ENST00000558518.6:c.1228A>G MANE Select	ENSP00000454071.1:p.Arg410Gly
ENST00000252444.9:c.1482A>G
ENST00000455727.6:c.724A>G	ENSP00000397829.2:p.Arg242Gly
ENST00000535915.5:c.1105A>G	ENSP00000440520.1:p.Arg369Gly
ENST00000545707.5:c.847A>G	ENSP00000437639.1:p.Arg283Gly
ENST00000557933.5:c.1228A>G	ENSP00000453557.1:p.Arg410Gly
ENST00000558013.5:c.1228A>G	ENSP00000453346.1:p.Arg410Gly
ENST00000558518.5:c.1228A>G	ENSP00000454071.1:p.Arg410Gly
ENST00000560173.1:n.227A>G
ENST00000560467.1:c.708A>G
NM_000527.4:c.1228A>G , LRG_274t1:c.1228A>G	NP_000518.1:p.Arg410Gly
NM_001195798.1:c.1228A>G	NP_001182727.1:p.Arg410Gly
NM_001195799.1:c.1105A>G	NP_001182728.1:p.Arg369Gly
NM_001195800.1:c.724A>G	NP_001182729.1:p.Arg242Gly
NM_001195803.1:c.847A>G	NP_001182732.1:p.Arg283Gly
XM_011528010.1:c.1228A>G	XP_011526312.1:p.Arg410Gly
XM_011528011.1:c.847A>G	XP_011526313.1:p.Arg283Gly
XR_244074.2:n.1378A>G
XM_011528010.2:c.1228A>G	XP_011526312.1:p.Arg410Gly
XR_001753685.2:n.1345A>G
XR_001753686.2:n.1345A>G
NM_000527.5:c.1228A>G MANE Select	NP_000518.1:p.Arg410Gly
NM_001195798.2:c.1228A>G	NP_001182727.1:p.Arg410Gly
NM_001195799.2:c.1105A>G	NP_001182728.1:p.Arg369Gly
NM_001195800.2:c.724A>G	NP_001182729.1:p.Arg242Gly
NM_001195803.2:c.847A>G	NP_001182732.1:p.Arg283Gly