Canonical Allele Identifier: CA404080622

Gene: LDLR

Linked Data

• ClinVar Variation Id: 1466547
• ClinVar RCV Id: RCV001966101 ; RCV003318707
• dbSNP Id: rs2077311848
• gnomAD v4: 19-11107419-T-C
• MyVariant Identifiers: chr19:g.11218095T>C (hg19) ; chr19:g.11107419T>C (hg38)
• ERepo: CA404080622/MONDO:0007750/013

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107419T>C , CM000681.2:g.11107419T>C	GRCh38
NC_000019.9:g.11218095T>C , CM000681.1:g.11218095T>C	GRCh37
NC_000019.8:g.11079095T>C	NCBI36
NG_009060.1:g.23039T>C , LRG_274:g.23039T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1103T>C	ENSP00000252444.6:p.Phe368Ser
ENST00000559340.2:c.845T>C	ENSP00000453696.2:p.Phe282Ser
ENST00000560467.2:c.845T>C	ENSP00000453513.2:p.Phe282Ser
ENST00000558518.6:c.845T>C MANE Select	ENSP00000454071.1:p.Phe282Ser
ENST00000252444.9:c.1099T>C
ENST00000455727.6:c.341T>C	ENSP00000397829.2:p.Phe114Ser
ENST00000535915.5:c.722T>C	ENSP00000440520.1:p.Phe241Ser
ENST00000545707.5:c.464T>C	ENSP00000437639.1:p.Phe155Ser
ENST00000557933.5:c.845T>C	ENSP00000453557.1:p.Phe282Ser
ENST00000558013.5:c.845T>C	ENSP00000453346.1:p.Phe282Ser
ENST00000558518.5:c.845T>C	ENSP00000454071.1:p.Phe282Ser
ENST00000558528.1:n.360T>C
ENST00000560467.1:c.445T>C
NM_000527.4:c.845T>C , LRG_274t1:c.845T>C	NP_000518.1:p.Phe282Ser
NM_001195798.1:c.845T>C	NP_001182727.1:p.Phe282Ser
NM_001195799.1:c.722T>C	NP_001182728.1:p.Phe241Ser
NM_001195800.1:c.341T>C	NP_001182729.1:p.Phe114Ser
NM_001195803.1:c.464T>C	NP_001182732.1:p.Phe155Ser
XM_011528010.1:c.845T>C	XP_011526312.1:p.Phe282Ser
XM_011528011.1:c.464T>C	XP_011526313.1:p.Phe155Ser
XR_244074.2:n.995T>C
XM_011528010.2:c.845T>C	XP_011526312.1:p.Phe282Ser
XR_001753685.2:n.962T>C
XR_001753686.2:n.962T>C
NM_000527.5:c.845T>C MANE Select	NP_000518.1:p.Phe282Ser
NM_001195798.2:c.845T>C	NP_001182727.1:p.Phe282Ser
NM_001195799.2:c.722T>C	NP_001182728.1:p.Phe241Ser
NM_001195800.2:c.341T>C	NP_001182729.1:p.Phe114Ser
NM_001195803.2:c.464T>C	NP_001182732.1:p.Phe155Ser