Canonical Allele Identifier: CA404093896

Gene: LDLR

Linked Data

• ClinVar Variation Id: 548083
• ClinVar RCV Id: RCV000660721
• dbSNP Id: rs1555807442
• MyVariant Identifiers: chr19:g.11231150T>G (hg19) ; chr19:g.11120474T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120474T>G , CM000681.2:g.11120474T>G	GRCh38
NC_000019.9:g.11231150T>G , CM000681.1:g.11231150T>G	GRCh37
NC_000019.8:g.11092150T>G	NCBI36
NG_009060.1:g.36094T>G , LRG_274:g.36094T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2350T>G	ENSP00000252444.6:p.Cys784Gly
ENST00000559340.2:c.*161T>G	ENSP00000453696.2:n.*161T>G
ENST00000560467.2:c.1972T>G	ENSP00000453513.2:p.Cys658Gly
ENST00000558518.6:c.2092T>G MANE Select	ENSP00000454071.1:p.Cys698Gly
ENST00000252444.9:c.2346T>G
ENST00000455727.6:c.1588T>G	ENSP00000397829.2:p.Cys530Gly
ENST00000535915.5:c.1969T>G	ENSP00000440520.1:p.Cys657Gly
ENST00000545707.5:c.1606+241T>G	ENSP00000437639.1:n.1606+241T>G
ENST00000557933.5:c.2092T>G	ENSP00000453557.1:p.Cys698Gly
ENST00000558013.5:c.2092T>G	ENSP00000453346.1:p.Cys698Gly
ENST00000558518.5:c.2092T>G	ENSP00000454071.1:p.Cys698Gly
NM_000527.4:c.2092T>G , LRG_274t1:c.2092T>G	NP_000518.1:p.Cys698Gly
NM_001195798.1:c.2092T>G	NP_001182727.1:p.Cys698Gly
NM_001195799.1:c.1969T>G	NP_001182728.1:p.Cys657Gly
NM_001195800.1:c.1588T>G	NP_001182729.1:p.Cys530Gly
NM_001195803.1:c.1606+241T>G	NP_001182732.1:n.1606+241T>G
XM_011528010.1:c.2092T>G	XP_011526312.1:p.Cys698Gly
XM_011528011.1:c.1711T>G	XP_011526313.1:p.Cys571Gly
XR_244074.2:n.2102T>G
XM_011528010.2:c.2092T>G	XP_011526312.1:p.Cys698Gly
XR_001753685.2:n.2209T>G
XR_001753686.2:n.2069T>G
NM_000527.5:c.2092T>G MANE Select	NP_000518.1:p.Cys698Gly
NM_001195798.2:c.2092T>G	NP_001182727.1:p.Cys698Gly
NM_001195799.2:c.1969T>G	NP_001182728.1:p.Cys657Gly
NM_001195800.2:c.1588T>G	NP_001182729.1:p.Cys530Gly
NM_001195803.2:c.1606+241T>G	NP_001182732.1:n.1606+241T>G