Canonical Allele Identifier: CA2069500784
Gene: SCARB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124800130G= , CM000674.2:g.124800130G= GRCh38
NC_000012.11:g.125284676G= , CM000674.1:g.125284676G= GRCh37
NC_000012.10:g.123850629G= NCBI36
NG_028199.1:g.68844C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261693.11:c.1122C= MANE Select ENSP00000261693.6:p.Ile374=
ENST00000679605.1:c.*128+7631C= ENSP00000505370.1:n.*128+7631C=
ENST00000679955.1:n.2846C=
ENST00000680556.1:c.1004+7636C= ENSP00000505757.1:n.1004+7636C=
ENST00000680596.1:c.1098C= ENSP00000505605.1:p.Ile366=
ENST00000680926.1:c.*70C= ENSP00000505571.1:n.*70C=
ENST00000680982.1:c.*1105C= ENSP00000506281.1:n.*1105C=
ENST00000681117.1:c.*241C= ENSP00000506693.1:n.*241C=
ENST00000681499.1:n.995C=
ENST00000681555.1:n.812C=
ENST00000681686.1:c.1122C= ENSP00000505406.1:p.Ile374=
ENST00000261693.10:c.1122C= ENSP00000261693.6:p.Ile374=
ENST00000339570.9:c.1122C= ENSP00000343795.4:p.Ile374=
ENST00000415380.6:c.1122C= ENSP00000414979.2:p.Ile374=
ENST00000535005.5:n.1437C=
ENST00000538291.5:n.1265C=
ENST00000544327.1:c.960C= ENSP00000444851.1:p.Ile320=
ENST00000546215.5:c.1122C= ENSP00000442862.1:p.Ile374=
NM_001082959.1:c.1122C= NP_001076428.1:p.Ile374=
NM_005505.4:c.1122C= NP_005496.4:p.Ile374=
NM_005505.5:c.1122C= MANE Select NP_005496.4:p.Ile374=
NM_001082959.2:c.1122C= NP_001076428.1:p.Ile374=
NM_001367981.1:c.1122C= NP_001354910.1:p.Ile374=
NM_001367982.1:c.999C= NP_001354911.1:p.Ile333=
NM_001367983.1:c.1122C= NP_001354912.1:p.Ile374=
NM_001367984.1:c.1122C= NP_001354913.1:p.Ile374=
NM_001367985.1:c.1098C= NP_001354914.1:p.Ile366=
NM_001367986.1:c.1122C= NP_001354915.1:p.Ile374=
NM_001367987.1:c.1004+7636C= NP_001354916.1:n.1004+7636C=
NM_001367988.1:c.727-4862C= NP_001354917.1:n.727-4862C=
NM_001367989.1:c.1122C= NP_001354918.1:p.Ile374=
NR_160416.1:n.1266C=
NR_160417.1:n.1266C=
NR_160418.1:n.1037+7631C=
NR_160419.1:n.1266C=
NR_160420.1:n.1150C=
NR_160421.1:n.1153+7631C=
NR_160422.1:n.1150C=
NR_160423.1:n.1154-4862C=
NR_160424.1:n.1261C=