Canonical Allele Identifier: CA038192

Gene: LDLR

Linked Data

• ClinVar Variation Id: 252174
• ClinVar RCV Id: RCV000237209 ; RCV001171939 ; RCV002057264 ; RCV002418063
• dbSNP Id: rs778781895
• ExAC: 19:11231083 C / T
• gnomAD v2: 19-11231083-C-T
• gnomAD v4: 19-11120407-C-T
• MyVariant Identifiers: chr19:g.11231083C>T (hg19) ; chr19:g.11120407C>T (hg38)
• PubMed: PMID:26892515

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120407C>T , CM000681.2:g.11120407C>T	GRCh38
NC_000019.9:g.11231083C>T , CM000681.1:g.11231083C>T	GRCh37
NC_000019.8:g.11092083C>T	NCBI36
NG_009060.1:g.36027C>T , LRG_274:g.36027C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2283C>T	ENSP00000252444.6:p.Gly761=
ENST00000559340.2:c.*94C>T	ENSP00000453696.2:n.*94C>T
ENST00000560467.2:c.1905C>T	ENSP00000453513.2:p.Gly635=
ENST00000558518.6:c.2025C>T MANE Select	ENSP00000454071.1:p.Gly675=
ENST00000252444.9:c.2279C>T
ENST00000455727.6:c.1521C>T	ENSP00000397829.2:p.Gly507=
ENST00000535915.5:c.1902C>T	ENSP00000440520.1:p.Gly634=
ENST00000545707.5:c.1606+174C>T	ENSP00000437639.1:n.1606+174C>T
ENST00000557933.5:c.2025C>T	ENSP00000453557.1:p.Gly675=
ENST00000558013.5:c.2025C>T	ENSP00000453346.1:p.Gly675=
ENST00000558518.5:c.2025C>T	ENSP00000454071.1:p.Gly675=
NM_000527.4:c.2025C>T , LRG_274t1:c.2025C>T	NP_000518.1:p.Gly675=
NM_001195798.1:c.2025C>T	NP_001182727.1:p.Gly675=
NM_001195799.1:c.1902C>T	NP_001182728.1:p.Gly634=
NM_001195800.1:c.1521C>T	NP_001182729.1:p.Gly507=
NM_001195803.1:c.1606+174C>T	NP_001182732.1:n.1606+174C>T
XM_011528010.1:c.2025C>T	XP_011526312.1:p.Gly675=
XM_011528011.1:c.1644C>T	XP_011526313.1:p.Gly548=
XR_244074.2:n.2035C>T
XM_011528010.2:c.2025C>T	XP_011526312.1:p.Gly675=
XR_001753685.2:n.2142C>T
XR_001753686.2:n.2002C>T
NM_000527.5:c.2025C>T MANE Select	NP_000518.1:p.Gly675=
NM_001195798.2:c.2025C>T	NP_001182727.1:p.Gly675=
NM_001195799.2:c.1902C>T	NP_001182728.1:p.Gly634=
NM_001195800.2:c.1521C>T	NP_001182729.1:p.Gly507=
NM_001195803.2:c.1606+174C>T	NP_001182732.1:n.1606+174C>T