Canonical Allele Identifier: CA783240929

Gene: LDLR

Linked Data

• dbSNP Id: rs1243408344
• gnomAD v4: 19-11111700-G-A
• MyVariant Identifiers: chr19:g.11222376G>A (hg19) ; chr19:g.11111700G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11111700G>A , CM000681.2:g.11111700G>A	GRCh38
NC_000019.9:g.11222376G>A , CM000681.1:g.11222376G>A	GRCh37
NC_000019.8:g.11083376G>A	NCBI36
NG_009060.1:g.27320G>A , LRG_274:g.27320G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1444+61G>A	ENSP00000252444.6:n.1444+61G>A
ENST00000559340.2:c.1186+61G>A	ENSP00000453696.2:n.1186+61G>A
ENST00000560467.2:c.1066+61G>A	ENSP00000453513.2:n.1066+61G>A
ENST00000558518.6:c.1186+61G>A MANE Select	ENSP00000454071.1:n.1186+61G>A
ENST00000252444.9:c.1440+61G>A
ENST00000455727.6:c.682+61G>A	ENSP00000397829.2:n.682+61G>A
ENST00000535915.5:c.1063+61G>A	ENSP00000440520.1:n.1063+61G>A
ENST00000545707.5:c.805+61G>A	ENSP00000437639.1:n.805+61G>A
ENST00000557933.5:c.1186+61G>A	ENSP00000453557.1:n.1186+61G>A
ENST00000558013.5:c.1186+61G>A	ENSP00000453346.1:n.1186+61G>A
ENST00000558518.5:c.1186+61G>A	ENSP00000454071.1:n.1186+61G>A
ENST00000560173.1:n.185+61G>A
ENST00000560467.1:c.666+61G>A
NM_000527.4:c.1186+61G>A , LRG_274t1:c.1186+61G>A	NP_000518.1:n.1186+61G>A
NM_001195798.1:c.1186+61G>A	NP_001182727.1:n.1186+61G>A
NM_001195799.1:c.1063+61G>A	NP_001182728.1:n.1063+61G>A
NM_001195800.1:c.682+61G>A	NP_001182729.1:n.682+61G>A
NM_001195803.1:c.805+61G>A	NP_001182732.1:n.805+61G>A
XM_011528010.1:c.1186+61G>A	XP_011526312.1:n.1186+61G>A
XM_011528011.1:c.805+61G>A	XP_011526313.1:n.805+61G>A
XR_244074.2:n.1336+61G>A
XM_011528010.2:c.1186+61G>A	XP_011526312.1:n.1186+61G>A
XR_001753685.2:n.1303+61G>A
XR_001753686.2:n.1303+61G>A
NM_000527.5:c.1186+61G>A MANE Select	NP_000518.1:n.1186+61G>A
NM_001195798.2:c.1186+61G>A	NP_001182727.1:n.1186+61G>A
NM_001195799.2:c.1063+61G>A	NP_001182728.1:n.1063+61G>A
NM_001195800.2:c.682+61G>A	NP_001182729.1:n.682+61G>A
NM_001195803.2:c.805+61G>A	NP_001182732.1:n.805+61G>A