Canonical Allele Identifier: CA220550528

Gene: LDLRAD3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36185122C>T , CM000673.2:g.36185122C>T	GRCh38
NC_000011.9:g.36206672C>T , CM000673.1:g.36206672C>T	GRCh37
NC_000011.8:g.36163248C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315571.6:c.455-41963C>T MANE Select	ENSP00000318607.5:n.455-41963C>T
ENST00000315571.5:c.455-41963C>T	ENSP00000318607.5:n.455-41963C>T
ENST00000524419.5:c.425-41963C>T	ENSP00000434313.1:n.425-41963C>T
ENST00000528989.5:c.308-41963C>T	ENSP00000433954.1:n.308-41963C>T
ENST00000529759.1:n.292+21532C>T
ENST00000532490.1:n.409-44038C>T
ENST00000534091.1:n.171-41963C>T
NM_001304263.1:c.308-41963C>T	NP_001291192.1:n.308-41963C>T
NM_001304264.1:c.91+1014C>T	NP_001291193.1:n.91+1014C>T
NM_174902.3:c.455-41963C>T	NP_777562.1:n.455-41963C>T
NM_174902.4:c.455-41963C>T MANE Select	NP_777562.1:n.455-41963C>T
NM_001304263.2:c.308-41963C>T	NP_001291192.1:n.308-41963C>T
NM_001304264.2:c.91+1014C>T	NP_001291193.1:n.91+1014C>T