Canonical Allele Identifier: CA2322767809
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105910_11105913delinsTTTG , CM000681.2:g.11105910_11105913delinsTTTG GRCh38
NC_000019.9:g.11216586_11216589delinsTTTG , CM000681.1:g.11216586_11216589delinsTTTG GRCh37
NC_000019.8:g.11077586_11077589delinsTTTG NCBI36
NG_009060.1:g.21530_21533delinsTTTG , LRG_274:g.21530_21533delinsTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.952+310_952+313delinsTTTG ENSP00000252444.6:n.952+310_952+313delinsTTTG
ENST00000559340.2:c.694+310_694+313delinsTTTG ENSP00000453696.2:n.694+310_694+313delinsTTTG
ENST00000560467.2:c.694+310_694+313delinsTTTG ENSP00000453513.2:n.694+310_694+313delinsTTTG
ENST00000558518.6:c.694+310_694+313delinsTTTG MANE Select ENSP00000454071.1:n.694+310_694+313delinsTTTG
ENST00000252444.9:c.948+310_948+313delinsTTTG
ENST00000455727.6:c.314-1482_314-1479delinsTTTG ENSP00000397829.2:n.314-1482_314-1479delinsTTTG
ENST00000535915.5:c.571+310_571+313delinsTTTG ENSP00000440520.1:n.571+310_571+313delinsTTTG
ENST00000545707.5:c.314-655_314-652delinsTTTG ENSP00000437639.1:n.314-655_314-652delinsTTTG
ENST00000557933.5:c.694+310_694+313delinsTTTG ENSP00000453557.1:n.694+310_694+313delinsTTTG
ENST00000558013.5:c.694+310_694+313delinsTTTG ENSP00000453346.1:n.694+310_694+313delinsTTTG
ENST00000558518.5:c.694+310_694+313delinsTTTG ENSP00000454071.1:n.694+310_694+313delinsTTTG
ENST00000560467.1:c.294+310_294+313delinsTTTG
NM_000527.4:c.694+310_694+313delinsTTTG , LRG_274t1:c.694+310_694+313delinsTTTG NP_000518.1:n.694+310_694+313delinsTTTG
NM_001195798.1:c.694+310_694+313delinsTTTG NP_001182727.1:n.694+310_694+313delinsTTTG
NM_001195799.1:c.571+310_571+313delinsTTTG NP_001182728.1:n.571+310_571+313delinsTTTG
NM_001195800.1:c.314-1482_314-1479delinsTTTG NP_001182729.1:n.314-1482_314-1479delinsTTTG
NM_001195803.1:c.314-655_314-652delinsTTTG NP_001182732.1:n.314-655_314-652delinsTTTG
XM_011528010.1:c.694+310_694+313delinsTTTG XP_011526312.1:n.694+310_694+313delinsTTTG
XM_011528011.1:c.314-655_314-652delinsTTTG XP_011526313.1:n.314-655_314-652delinsTTTG
XR_244074.2:n.844+310_844+313delinsTTTG
XM_011528010.2:c.694+310_694+313delinsTTTG XP_011526312.1:n.694+310_694+313delinsTTTG
XR_001753685.2:n.811+310_811+313delinsTTTG
XR_001753686.2:n.811+310_811+313delinsTTTG
NM_000527.5:c.694+310_694+313delinsTTTG MANE Select NP_000518.1:n.694+310_694+313delinsTTTG
NM_001195798.2:c.694+310_694+313delinsTTTG NP_001182727.1:n.694+310_694+313delinsTTTG
NM_001195799.2:c.571+310_571+313delinsTTTG NP_001182728.1:n.571+310_571+313delinsTTTG
NM_001195800.2:c.314-1482_314-1479delinsTTTG NP_001182729.1:n.314-1482_314-1479delinsTTTG
NM_001195803.2:c.314-655_314-652delinsTTTG NP_001182732.1:n.314-655_314-652delinsTTTG