Canonical Allele Identifier: CA404095888

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11234020G>T (hg19) ; chr19:g.11123344G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11123344G>T , CM000681.2:g.11123344G>T	GRCh38
NC_000019.9:g.11234020G>T , CM000681.1:g.11234020G>T	GRCh37
NC_000019.8:g.11095020G>T	NCBI36
NG_009060.1:g.38964G>T , LRG_274:g.38964G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2569G>T	ENSP00000252444.6:p.Ala857Ser
ENST00000559340.2:c.*380G>T	ENSP00000453696.2:n.*380G>T
ENST00000560467.2:c.2191G>T	ENSP00000453513.2:p.Ala731Ser
ENST00000558518.6:c.2311G>T MANE Select	ENSP00000454071.1:p.Ala771Ser
ENST00000252444.9:c.2565G>T
ENST00000455727.6:c.1807G>T	ENSP00000397829.2:p.Ala603Ser
ENST00000535915.5:c.2188G>T	ENSP00000440520.1:p.Ala730Ser
ENST00000545707.5:c.1777G>T	ENSP00000437639.1:p.Ala593Ser
ENST00000557933.5:c.2311G>T	ENSP00000453557.1:p.Ala771Ser
ENST00000558013.5:c.2311G>T	ENSP00000453346.1:p.Ala771Ser
ENST00000558518.5:c.2311G>T	ENSP00000454071.1:p.Ala771Ser
NM_000527.4:c.2311G>T , LRG_274t1:c.2311G>T	NP_000518.1:p.Ala771Ser
NM_001195798.1:c.2311G>T	NP_001182727.1:p.Ala771Ser
NM_001195799.1:c.2188G>T	NP_001182728.1:p.Ala730Ser
NM_001195800.1:c.1807G>T	NP_001182729.1:p.Ala603Ser
NM_001195803.1:c.1777G>T	NP_001182732.1:p.Ala593Ser
XM_011528010.1:c.2311G>T	XP_011526312.1:p.Val771Leu
XM_011528011.1:c.1930G>T	XP_011526313.1:p.Ala644Ser
XR_244074.2:n.2321G>T
XM_011528010.2:c.2311G>T	XP_011526312.1:p.Val771Leu
XR_001753685.2:n.2645G>T
XR_001753686.2:n.2288G>T
NM_000527.5:c.2311G>T MANE Select	NP_000518.1:p.Ala771Ser
NM_001195798.2:c.2311G>T	NP_001182727.1:p.Ala771Ser
NM_001195799.2:c.2188G>T	NP_001182728.1:p.Ala730Ser
NM_001195800.2:c.1807G>T	NP_001182729.1:p.Ala603Ser
NM_001195803.2:c.1777G>T	NP_001182732.1:p.Ala593Ser