Canonical Allele Identifier: CA2621767687

Gene: SCARB1

Linked Data

• gnomAD v4: 12-124776906-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124776910del , CM000674.2:g.124776910del	GRCh38
NC_000012.11:g.125261456del , CM000674.1:g.125261456del	GRCh37
NC_000012.10:g.123827409del	NCBI36
NG_028199.1:g.92067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1680del MANE Select	ENSP00000261693.6:n.*1680del
ENST00000339570.9:c.*1560del	ENSP00000343795.4:n.*1560del
NM_005505.5:c.*1680del MANE Select	NP_005496.4:n.*1680del
NM_001082959.2:c.*1560del	NP_001076428.1:n.*1560del
NM_001367981.1:c.*1672del	NP_001354910.1:n.*1672del
NM_001367983.1:c.*1680del	NP_001354912.1:n.*1680del
NM_001367984.1:c.*1680del	NP_001354913.1:n.*1680del
NM_001367985.1:c.*1680del	NP_001354914.1:n.*1680del
NM_001367986.1:c.*1680del	NP_001354915.1:n.*1680del
NM_001367987.1:c.*1560del	NP_001354916.1:n.*1560del
NM_001367988.1:c.*1680del	NP_001354917.1:n.*1680del
NM_001367989.1:c.*1691del	NP_001354918.1:n.*1691del
NR_160416.1:n.3355del
NR_160417.1:n.3457del
NR_160418.1:n.2916del
NR_160419.1:n.3280del
NR_160420.1:n.3109del
NR_160421.1:n.3032del
NR_160422.1:n.3238del
NR_160423.1:n.3235del
NR_160424.1:n.3220del