Canonical Allele Identifier: CA505487462
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11238697T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128021T>A , CM000681.2:g.11128021T>A GRCh38
NC_000019.9:g.11238697T>A , CM000681.1:g.11238697T>A GRCh37
NC_000019.8:g.11099697T>A NCBI36
NG_009060.1:g.43641T>A , LRG_274:g.43641T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2583T>A ENSP00000252444.6:p.Val861=
ENST00000559340.2:c.*394T>A ENSP00000453696.2:n.*394T>A
ENST00000560467.2:c.2205T>A ENSP00000453513.2:p.Val735=
ENST00000558518.6:c.2325T>A MANE Select ENSP00000454071.1:p.Val775=
ENST00000252444.9:c.2579T>A
ENST00000455727.6:c.1821T>A ENSP00000397829.2:p.Val607=
ENST00000535915.5:c.2202T>A ENSP00000440520.1:p.Val734=
ENST00000545707.5:c.1791T>A ENSP00000437639.1:p.Val597=
ENST00000557933.5:c.2325T>A ENSP00000453557.1:p.Val775=
ENST00000558013.5:c.2325T>A ENSP00000453346.1:p.Val775=
ENST00000558518.5:c.2325T>A ENSP00000454071.1:p.Val775=
ENST00000560628.1:n.108+367T>A
NM_000527.4:c.2325T>A , LRG_274t1:c.2325T>A NP_000518.1:p.Val775=
NM_001195798.1:c.2325T>A NP_001182727.1:p.Val775=
NM_001195799.1:c.2202T>A NP_001182728.1:p.Val734=
NM_001195800.1:c.1821T>A NP_001182729.1:p.Val607=
NM_001195803.1:c.1791T>A NP_001182732.1:p.Val597=
XM_011528010.1:c.2312-1492T>A XP_011526312.1:n.2312-1492T>A
XM_011528011.1:c.1944T>A XP_011526313.1:p.Val648=
XR_244074.2:n.2335T>A
XM_011528010.2:c.2312-1492T>A XP_011526312.1:n.2312-1492T>A
XR_001753685.2:n.2659T>A
XR_001753686.2:n.2302T>A
NM_000527.5:c.2325T>A MANE Select NP_000518.1:p.Val775=
NM_001195798.2:c.2325T>A NP_001182727.1:p.Val775=
NM_001195799.2:c.2202T>A NP_001182728.1:p.Val734=
NM_001195800.2:c.1821T>A NP_001182729.1:p.Val607=
NM_001195803.2:c.1791T>A NP_001182732.1:p.Val597=