Canonical Allele Identifier: CA2069500612
Gene: SCARB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124800039_124800041delinsGCT , CM000674.2:g.124800039_124800041delinsGCT GRCh38
NC_000012.11:g.125284585_125284587delinsGCT , CM000674.1:g.125284585_125284587delinsGCT GRCh37
NC_000012.10:g.123850538_123850540delinsGCT NCBI36
NG_028199.1:g.68933_68935delinsAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000261693.11:c.1128+83_1128+85delinsAGC MANE Select ENSP00000261693.6:n.1128+83_1128+85delinsAGC
ENST00000679605.1:c.*128+7720_*128+7722delinsAGC ENSP00000505370.1:n.*128+7720_*128+7722delinsAGC
ENST00000679955.1:n.2852+83_2852+85delinsAGC
ENST00000680556.1:c.1004+7725_1004+7727delinsAGC ENSP00000505757.1:n.1004+7725_1004+7727delinsAGC
ENST00000680596.1:c.1104+83_1104+85delinsAGC ENSP00000505605.1:n.1104+83_1104+85delinsAGC
ENST00000680926.1:c.*76+83_*76+85delinsAGC ENSP00000505571.1:n.*76+83_*76+85delinsAGC
ENST00000680982.1:c.*1111+83_*1111+85delinsAGC ENSP00000506281.1:n.*1111+83_*1111+85delinsAGC
ENST00000681117.1:c.*247+83_*247+85delinsAGC ENSP00000506693.1:n.*247+83_*247+85delinsAGC
ENST00000681499.1:n.1001+83_1001+85delinsAGC
ENST00000681555.1:n.818+83_818+85delinsAGC
ENST00000681686.1:c.1128+83_1128+85delinsAGC ENSP00000505406.1:n.1128+83_1128+85delinsAGC
ENST00000261693.10:c.1128+83_1128+85delinsAGC ENSP00000261693.6:n.1128+83_1128+85delinsAGC
ENST00000339570.9:c.1128+83_1128+85delinsAGC ENSP00000343795.4:n.1128+83_1128+85delinsAGC
ENST00000415380.6:c.1128+83_1128+85delinsAGC ENSP00000414979.2:n.1128+83_1128+85delinsAGC
ENST00000535005.5:n.1443+83_1443+85delinsAGC
ENST00000538291.5:n.1271+83_1271+85delinsAGC
ENST00000544327.1:c.966+83_966+85delinsAGC ENSP00000444851.1:n.966+83_966+85delinsAGC
ENST00000546215.5:c.1128+83_1128+85delinsAGC ENSP00000442862.1:n.1128+83_1128+85delinsAGC
NM_001082959.1:c.1128+83_1128+85delinsAGC NP_001076428.1:n.1128+83_1128+85delinsAGC
NM_005505.4:c.1128+83_1128+85delinsAGC NP_005496.4:n.1128+83_1128+85delinsAGC
NM_005505.5:c.1128+83_1128+85delinsAGC MANE Select NP_005496.4:n.1128+83_1128+85delinsAGC
NM_001082959.2:c.1128+83_1128+85delinsAGC NP_001076428.1:n.1128+83_1128+85delinsAGC
NM_001367981.1:c.1128+83_1128+85delinsAGC NP_001354910.1:n.1128+83_1128+85delinsAGC
NM_001367982.1:c.1005+83_1005+85delinsAGC NP_001354911.1:n.1005+83_1005+85delinsAGC
NM_001367983.1:c.1128+83_1128+85delinsAGC NP_001354912.1:n.1128+83_1128+85delinsAGC
NM_001367984.1:c.1128+83_1128+85delinsAGC NP_001354913.1:n.1128+83_1128+85delinsAGC
NM_001367985.1:c.1104+83_1104+85delinsAGC NP_001354914.1:n.1104+83_1104+85delinsAGC
NM_001367986.1:c.1128+83_1128+85delinsAGC NP_001354915.1:n.1128+83_1128+85delinsAGC
NM_001367987.1:c.1004+7725_1004+7727delinsAGC NP_001354916.1:n.1004+7725_1004+7727delinsAGC
NM_001367988.1:c.727-4773_727-4771delinsAGC NP_001354917.1:n.727-4773_727-4771delinsAGC
NM_001367989.1:c.1128+83_1128+85delinsAGC NP_001354918.1:n.1128+83_1128+85delinsAGC
NR_160416.1:n.1272+83_1272+85delinsAGC
NR_160417.1:n.1272+83_1272+85delinsAGC
NR_160418.1:n.1037+7720_1037+7722delinsAGC
NR_160419.1:n.1272+83_1272+85delinsAGC
NR_160420.1:n.1156+83_1156+85delinsAGC
NR_160421.1:n.1153+7720_1153+7722delinsAGC
NR_160422.1:n.1156+83_1156+85delinsAGC
NR_160423.1:n.1154-4773_1154-4771delinsAGC
NR_160424.1:n.1267+83_1267+85delinsAGC