Canonical Allele Identifier: CA404081038

Gene: LDLR

Linked Data

• ClinVar Variation Id: 440612
• ClinVar RCV Id: RCV000508931 ; RCV002376948
• dbSNP Id: rs121908030
• gnomAD v4: 19-11107484-G-C
• MyVariant Identifiers: chr19:g.11218160G>C (hg19) ; chr19:g.11107484G>C (hg38)
• ERepo: CA404081038/MONDO:0007750/013

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107484G>C , CM000681.2:g.11107484G>C	GRCh38
NC_000019.9:g.11218160G>C , CM000681.1:g.11218160G>C	GRCh37
NC_000019.8:g.11079160G>C	NCBI36
NG_009060.1:g.23104G>C , LRG_274:g.23104G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1168G>C	ENSP00000252444.6:p.Asp390His
ENST00000559340.2:c.910G>C	ENSP00000453696.2:p.Asp304His
ENST00000560467.2:c.910G>C	ENSP00000453513.2:p.Asp304His
ENST00000558518.6:c.910G>C MANE Select	ENSP00000454071.1:p.Asp304His
ENST00000252444.9:c.1164G>C
ENST00000455727.6:c.406G>C	ENSP00000397829.2:p.Asp136His
ENST00000535915.5:c.787G>C	ENSP00000440520.1:p.Asp263His
ENST00000545707.5:c.529G>C	ENSP00000437639.1:p.Asp177His
ENST00000557933.5:c.910G>C	ENSP00000453557.1:p.Asp304His
ENST00000558013.5:c.910G>C	ENSP00000453346.1:p.Asp304His
ENST00000558518.5:c.910G>C	ENSP00000454071.1:p.Asp304His
ENST00000558528.1:n.425G>C
ENST00000560467.1:c.510G>C
NM_000527.4:c.910G>C , LRG_274t1:c.910G>C	NP_000518.1:p.Asp304His
NM_001195798.1:c.910G>C	NP_001182727.1:p.Asp304His
NM_001195799.1:c.787G>C	NP_001182728.1:p.Asp263His
NM_001195800.1:c.406G>C	NP_001182729.1:p.Asp136His
NM_001195803.1:c.529G>C	NP_001182732.1:p.Asp177His
XM_011528010.1:c.910G>C	XP_011526312.1:p.Asp304His
XM_011528011.1:c.529G>C	XP_011526313.1:p.Asp177His
XR_244074.2:n.1060G>C
XM_011528010.2:c.910G>C	XP_011526312.1:p.Asp304His
XR_001753685.2:n.1027G>C
XR_001753686.2:n.1027G>C
NM_000527.5:c.910G>C MANE Select	NP_000518.1:p.Asp304His
NM_001195798.2:c.910G>C	NP_001182727.1:p.Asp304His
NM_001195799.2:c.787G>C	NP_001182728.1:p.Asp263His
NM_001195800.2:c.406G>C	NP_001182729.1:p.Asp136His
NM_001195803.2:c.529G>C	NP_001182732.1:p.Asp177His