Canonical Allele Identifier: CA305301175

Gene: LDLR

Linked Data

• dbSNP Id: rs192094774
• gnomAD v2: 19-11225435-G-T
• gnomAD v3: 19-11114759-G-T
• gnomAD v4: 19-11114759-G-T
• MyVariant Identifiers: chr19:g.11225435G>T (hg19) ; chr19:g.11114759G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11114759G>T , CM000681.2:g.11114759G>T	GRCh38
NC_000019.9:g.11225435G>T , CM000681.1:g.11225435G>T	GRCh37
NC_000019.8:g.11086435G>T	NCBI36
NG_009060.1:g.30379G>T , LRG_274:g.30379G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1844+997G>T	ENSP00000252444.6:n.1844+997G>T
ENST00000559340.2:c.1586+997G>T	ENSP00000453696.2:n.1586+997G>T
ENST00000560467.2:c.1466+997G>T	ENSP00000453513.2:n.1466+997G>T
ENST00000558518.6:c.1586+997G>T MANE Select	ENSP00000454071.1:n.1586+997G>T
ENST00000252444.9:c.1840+997G>T
ENST00000455727.6:c.1082+997G>T	ENSP00000397829.2:n.1082+997G>T
ENST00000535915.5:c.1463+997G>T	ENSP00000440520.1:n.1463+997G>T
ENST00000545707.5:c.1205+997G>T	ENSP00000437639.1:n.1205+997G>T
ENST00000557933.5:c.1586+997G>T	ENSP00000453557.1:n.1586+997G>T
ENST00000558013.5:c.1586+997G>T	ENSP00000453346.1:n.1586+997G>T
ENST00000558518.5:c.1586+997G>T	ENSP00000454071.1:n.1586+997G>T
ENST00000559340.1:c.307+997G>T
NM_000527.4:c.1586+997G>T , LRG_274t1:c.1586+997G>T	NP_000518.1:n.1586+997G>T
NM_001195798.1:c.1586+997G>T	NP_001182727.1:n.1586+997G>T
NM_001195799.1:c.1463+997G>T	NP_001182728.1:n.1463+997G>T
NM_001195800.1:c.1082+997G>T	NP_001182729.1:n.1082+997G>T
NM_001195803.1:c.1205+997G>T	NP_001182732.1:n.1205+997G>T
XM_011528010.1:c.1586+997G>T	XP_011526312.1:n.1586+997G>T
XM_011528011.1:c.1205+997G>T	XP_011526313.1:n.1205+997G>T
XR_244074.2:n.1736+997G>T
XM_011528010.2:c.1586+997G>T	XP_011526312.1:n.1586+997G>T
XR_001753685.2:n.1703+997G>T
XR_001753686.2:n.1703+997G>T
NM_000527.5:c.1586+997G>T MANE Select	NP_000518.1:n.1586+997G>T
NM_001195798.2:c.1586+997G>T	NP_001182727.1:n.1586+997G>T
NM_001195799.2:c.1463+997G>T	NP_001182728.1:n.1463+997G>T
NM_001195800.2:c.1082+997G>T	NP_001182729.1:n.1082+997G>T
NM_001195803.2:c.1205+997G>T	NP_001182732.1:n.1205+997G>T