Canonical Allele Identifier: CA404082620

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11221342T>A (hg19) ; chr19:g.11110666T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11110666T>A , CM000681.2:g.11110666T>A	GRCh38
NC_000019.9:g.11221342T>A , CM000681.1:g.11221342T>A	GRCh37
NC_000019.8:g.11082342T>A	NCBI36
NG_009060.1:g.26286T>A , LRG_274:g.26286T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1213T>A	ENSP00000252444.6:p.Leu405Met
ENST00000559340.2:c.955T>A	ENSP00000453696.2:p.Leu319Met
ENST00000560467.2:c.941-848T>A	ENSP00000453513.2:n.941-848T>A
ENST00000558518.6:c.955T>A MANE Select	ENSP00000454071.1:p.Leu319Met
ENST00000252444.9:c.1209T>A
ENST00000455727.6:c.451T>A	ENSP00000397829.2:p.Leu151Met
ENST00000535915.5:c.832T>A	ENSP00000440520.1:p.Leu278Met
ENST00000545707.5:c.574T>A	ENSP00000437639.1:p.Leu192Met
ENST00000557933.5:c.955T>A	ENSP00000453557.1:p.Leu319Met
ENST00000558013.5:c.955T>A	ENSP00000453346.1:p.Leu319Met
ENST00000558518.5:c.955T>A	ENSP00000454071.1:p.Leu319Met
ENST00000560467.1:c.541-848T>A
NM_000527.4:c.955T>A , LRG_274t1:c.955T>A	NP_000518.1:p.Leu319Met
NM_001195798.1:c.955T>A	NP_001182727.1:p.Leu319Met
NM_001195799.1:c.832T>A	NP_001182728.1:p.Leu278Met
NM_001195800.1:c.451T>A	NP_001182729.1:p.Leu151Met
NM_001195803.1:c.574T>A	NP_001182732.1:p.Leu192Met
XM_011528010.1:c.955T>A	XP_011526312.1:p.Leu319Met
XM_011528011.1:c.574T>A	XP_011526313.1:p.Leu192Met
XR_244074.2:n.1105T>A
XM_011528010.2:c.955T>A	XP_011526312.1:p.Leu319Met
XR_001753685.2:n.1072T>A
XR_001753686.2:n.1072T>A
NM_000527.5:c.955T>A MANE Select	NP_000518.1:p.Leu319Met
NM_001195798.2:c.955T>A	NP_001182727.1:p.Leu319Met
NM_001195799.2:c.832T>A	NP_001182728.1:p.Leu278Met
NM_001195800.2:c.451T>A	NP_001182729.1:p.Leu151Met
NM_001195803.2:c.574T>A	NP_001182732.1:p.Leu192Met