Canonical Allele Identifier: CA404082700

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11221381C>T (hg19) ; chr19:g.11110705C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11110705C>T , CM000681.2:g.11110705C>T	GRCh38
NC_000019.9:g.11221381C>T , CM000681.1:g.11221381C>T	GRCh37
NC_000019.8:g.11082381C>T	NCBI36
NG_009060.1:g.26325C>T , LRG_274:g.26325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1252C>T	ENSP00000252444.6:p.Leu418Phe
ENST00000559340.2:c.994C>T	ENSP00000453696.2:p.Leu332Phe
ENST00000560467.2:c.941-809C>T	ENSP00000453513.2:n.941-809C>T
ENST00000558518.6:c.994C>T MANE Select	ENSP00000454071.1:p.Leu332Phe
ENST00000252444.9:c.1248C>T
ENST00000455727.6:c.490C>T	ENSP00000397829.2:p.Leu164Phe
ENST00000535915.5:c.871C>T	ENSP00000440520.1:p.Leu291Phe
ENST00000545707.5:c.613C>T	ENSP00000437639.1:p.Leu205Phe
ENST00000557933.5:c.994C>T	ENSP00000453557.1:p.Leu332Phe
ENST00000558013.5:c.994C>T	ENSP00000453346.1:p.Leu332Phe
ENST00000558518.5:c.994C>T	ENSP00000454071.1:p.Leu332Phe
ENST00000560467.1:c.541-809C>T
NM_000527.4:c.994C>T , LRG_274t1:c.994C>T	NP_000518.1:p.Leu332Phe
NM_001195798.1:c.994C>T	NP_001182727.1:p.Leu332Phe
NM_001195799.1:c.871C>T	NP_001182728.1:p.Leu291Phe
NM_001195800.1:c.490C>T	NP_001182729.1:p.Leu164Phe
NM_001195803.1:c.613C>T	NP_001182732.1:p.Leu205Phe
XM_011528010.1:c.994C>T	XP_011526312.1:p.Leu332Phe
XM_011528011.1:c.613C>T	XP_011526313.1:p.Leu205Phe
XR_244074.2:n.1144C>T
XM_011528010.2:c.994C>T	XP_011526312.1:p.Leu332Phe
XR_001753685.2:n.1111C>T
XR_001753686.2:n.1111C>T
NM_000527.5:c.994C>T MANE Select	NP_000518.1:p.Leu332Phe
NM_001195798.2:c.994C>T	NP_001182727.1:p.Leu332Phe
NM_001195799.2:c.871C>T	NP_001182728.1:p.Leu291Phe
NM_001195800.2:c.490C>T	NP_001182729.1:p.Leu164Phe
NM_001195803.2:c.613C>T	NP_001182732.1:p.Leu205Phe