Canonical Allele Identifier: CA631763684

Gene: LDLR

Linked Data

• dbSNP Id: rs1568596274
• gnomAD v2: 19-11216617-G-GTTTTTA
• gnomAD v3: 19-11105941-G-GTTTTTA
• gnomAD v4: 19-11105941-G-GTTTTTA
• MyVariant Identifiers: chr19:g.11216617_11216618insTTTTTA (hg19) ; chr19:g.11105941_11105942insTTTTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11105945_11105946insTATTTT , CM000681.2:g.11105945_11105946insTATTTT	GRCh38
NC_000019.9:g.11216621_11216622insTATTTT , CM000681.1:g.11216621_11216622insTATTTT	GRCh37
NC_000019.8:g.11077621_11077622insTATTTT	NCBI36
NG_009060.1:g.21565_21566insTATTTT , LRG_274:g.21565_21566insTATTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.952+345_952+346insTATTTT	ENSP00000252444.6:n.952+345_952+346insTATTTT
ENST00000559340.2:c.694+345_694+346insTATTTT	ENSP00000453696.2:n.694+345_694+346insTATTTT
ENST00000560467.2:c.694+345_694+346insTATTTT	ENSP00000453513.2:n.694+345_694+346insTATTTT
ENST00000558518.6:c.694+345_694+346insTATTTT MANE Select	ENSP00000454071.1:n.694+345_694+346insTATTTT
ENST00000252444.9:c.948+345_948+346insTATTTT
ENST00000455727.6:c.314-1447_314-1446insTATTTT	ENSP00000397829.2:n.314-1447_314-1446insTATTTT
ENST00000535915.5:c.571+345_571+346insTATTTT	ENSP00000440520.1:n.571+345_571+346insTATTTT
ENST00000545707.5:c.314-620_314-619insTATTTT	ENSP00000437639.1:n.314-620_314-619insTATTTT
ENST00000557933.5:c.694+345_694+346insTATTTT	ENSP00000453557.1:n.694+345_694+346insTATTTT
ENST00000558013.5:c.694+345_694+346insTATTTT	ENSP00000453346.1:n.694+345_694+346insTATTTT
ENST00000558518.5:c.694+345_694+346insTATTTT	ENSP00000454071.1:n.694+345_694+346insTATTTT
ENST00000560467.1:c.294+345_294+346insTATTTT
NM_000527.4:c.694+345_694+346insTATTTT , LRG_274t1:c.694+345_694+346insTATTTT	NP_000518.1:n.694+345_694+346insTATTTT
NM_001195798.1:c.694+345_694+346insTATTTT	NP_001182727.1:n.694+345_694+346insTATTTT
NM_001195799.1:c.571+345_571+346insTATTTT	NP_001182728.1:n.571+345_571+346insTATTTT
NM_001195800.1:c.314-1447_314-1446insTATTTT	NP_001182729.1:n.314-1447_314-1446insTATTTT
NM_001195803.1:c.314-620_314-619insTATTTT	NP_001182732.1:n.314-620_314-619insTATTTT
XM_011528010.1:c.694+345_694+346insTATTTT	XP_011526312.1:n.694+345_694+346insTATTTT
XM_011528011.1:c.314-620_314-619insTATTTT	XP_011526313.1:n.314-620_314-619insTATTTT
XR_244074.2:n.844+345_844+346insTATTTT
XM_011528010.2:c.694+345_694+346insTATTTT	XP_011526312.1:n.694+345_694+346insTATTTT
XR_001753685.2:n.811+345_811+346insTATTTT
XR_001753686.2:n.811+345_811+346insTATTTT
NM_000527.5:c.694+345_694+346insTATTTT MANE Select	NP_000518.1:n.694+345_694+346insTATTTT
NM_001195798.2:c.694+345_694+346insTATTTT	NP_001182727.1:n.694+345_694+346insTATTTT
NM_001195799.2:c.571+345_571+346insTATTTT	NP_001182728.1:n.571+345_571+346insTATTTT
NM_001195800.2:c.314-1447_314-1446insTATTTT	NP_001182729.1:n.314-1447_314-1446insTATTTT
NM_001195803.2:c.314-620_314-619insTATTTT	NP_001182732.1:n.314-620_314-619insTATTTT