Canonical Allele Identifier: CA505485079

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11218123C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107447C>G , CM000681.2:g.11107447C>G	GRCh38
NC_000019.9:g.11218123C>G , CM000681.1:g.11218123C>G	GRCh37
NC_000019.8:g.11079123C>G	NCBI36
NG_009060.1:g.23067C>G , LRG_274:g.23067C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1131C>G	ENSP00000252444.6:p.Thr377=
ENST00000559340.2:c.873C>G	ENSP00000453696.2:p.Thr291=
ENST00000560467.2:c.873C>G	ENSP00000453513.2:p.Thr291=
ENST00000558518.6:c.873C>G MANE Select	ENSP00000454071.1:p.Thr291=
ENST00000252444.9:c.1127C>G
ENST00000455727.6:c.369C>G	ENSP00000397829.2:p.Thr123=
ENST00000535915.5:c.750C>G	ENSP00000440520.1:p.Thr250=
ENST00000545707.5:c.492C>G	ENSP00000437639.1:p.Thr164=
ENST00000557933.5:c.873C>G	ENSP00000453557.1:p.Thr291=
ENST00000558013.5:c.873C>G	ENSP00000453346.1:p.Thr291=
ENST00000558518.5:c.873C>G	ENSP00000454071.1:p.Thr291=
ENST00000558528.1:n.388C>G
ENST00000560467.1:c.473C>G
NM_000527.4:c.873C>G , LRG_274t1:c.873C>G	NP_000518.1:p.Thr291=
NM_001195798.1:c.873C>G	NP_001182727.1:p.Thr291=
NM_001195799.1:c.750C>G	NP_001182728.1:p.Thr250=
NM_001195800.1:c.369C>G	NP_001182729.1:p.Thr123=
NM_001195803.1:c.492C>G	NP_001182732.1:p.Thr164=
XM_011528010.1:c.873C>G	XP_011526312.1:p.Thr291=
XM_011528011.1:c.492C>G	XP_011526313.1:p.Thr164=
XR_244074.2:n.1023C>G
XM_011528010.2:c.873C>G	XP_011526312.1:p.Thr291=
XR_001753685.2:n.990C>G
XR_001753686.2:n.990C>G
NM_000527.5:c.873C>G MANE Select	NP_000518.1:p.Thr291=
NM_001195798.2:c.873C>G	NP_001182727.1:p.Thr291=
NM_001195799.2:c.750C>G	NP_001182728.1:p.Thr250=
NM_001195800.2:c.369C>G	NP_001182729.1:p.Thr123=
NM_001195803.2:c.492C>G	NP_001182732.1:p.Thr164=