Canonical Allele Identifier: CA2069464134

Gene: SCARB1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124776894_124776896delinsAGG , CM000674.2:g.124776894_124776896delinsAGG	GRCh38
NC_000012.11:g.125261440_125261442delinsAGG , CM000674.1:g.125261440_125261442delinsAGG	GRCh37
NC_000012.10:g.123827393_123827395delinsAGG	NCBI36
NG_028199.1:g.92078_92080delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1691_*1693delinsCCT MANE Select	ENSP00000261693.6:n.*1691_*1693delinsCCT
ENST00000339570.9:c.*1571_*1573delinsCCT	ENSP00000343795.4:n.*1571_*1573delinsCCT
NM_005505.5:c.*1691_*1693delinsCCT MANE Select	NP_005496.4:n.*1691_*1693delinsCCT
NM_001082959.2:c.*1571_*1573delinsCCT	NP_001076428.1:n.*1571_*1573delinsCCT
NM_001367981.1:c.*1683_*1685delinsCCT	NP_001354910.1:n.*1683_*1685delinsCCT
NM_001367983.1:c.*1691_*1693delinsCCT	NP_001354912.1:n.*1691_*1693delinsCCT
NM_001367984.1:c.*1691_*1693delinsCCT	NP_001354913.1:n.*1691_*1693delinsCCT
NM_001367985.1:c.*1691_*1693delinsCCT	NP_001354914.1:n.*1691_*1693delinsCCT
NM_001367986.1:c.*1691_*1693delinsCCT	NP_001354915.1:n.*1691_*1693delinsCCT
NM_001367987.1:c.*1571_*1573delinsCCT	NP_001354916.1:n.*1571_*1573delinsCCT
NM_001367988.1:c.*1691_*1693delinsCCT	NP_001354917.1:n.*1691_*1693delinsCCT
NM_001367989.1:c.*1702_*1704delinsCCT	NP_001354918.1:n.*1702_*1704delinsCCT
NR_160416.1:n.3366_3368delinsCCT
NR_160417.1:n.3468_3470delinsCCT
NR_160418.1:n.2927_2929delinsCCT
NR_160419.1:n.3291_3293delinsCCT
NR_160420.1:n.3120_3122delinsCCT
NR_160421.1:n.3043_3045delinsCCT
NR_160422.1:n.3249_3251delinsCCT
NR_160423.1:n.3246_3248delinsCCT
NR_160424.1:n.3231_3233delinsCCT