Canonical Allele Identifier: CA387213432
Gene: SCARB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124800129G>A , CM000674.2:g.124800129G>A GRCh38
NC_000012.11:g.125284675G>A , CM000674.1:g.125284675G>A GRCh37
NC_000012.10:g.123850628G>A NCBI36
NG_028199.1:g.68845C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261693.11:c.1123C>T MANE Select ENSP00000261693.6:p.His375Tyr
ENST00000679605.1:c.*128+7632C>T ENSP00000505370.1:n.*128+7632C>T
ENST00000679955.1:n.2847C>T
ENST00000680556.1:c.1004+7637C>T ENSP00000505757.1:n.1004+7637C>T
ENST00000680596.1:c.1099C>T ENSP00000505605.1:p.His367Tyr
ENST00000680926.1:c.*71C>T ENSP00000505571.1:n.*71C>T
ENST00000680982.1:c.*1106C>T ENSP00000506281.1:n.*1106C>T
ENST00000681117.1:c.*242C>T ENSP00000506693.1:n.*242C>T
ENST00000681499.1:n.996C>T
ENST00000681555.1:n.813C>T
ENST00000681686.1:c.1123C>T ENSP00000505406.1:p.His375Tyr
ENST00000261693.10:c.1123C>T ENSP00000261693.6:p.His375Tyr
ENST00000339570.9:c.1123C>T ENSP00000343795.4:p.His375Tyr
ENST00000415380.6:c.1123C>T ENSP00000414979.2:p.His375Tyr
ENST00000535005.5:n.1438C>T
ENST00000538291.5:n.1266C>T
ENST00000544327.1:c.961C>T ENSP00000444851.1:p.His321Tyr
ENST00000546215.5:c.1123C>T ENSP00000442862.1:p.His375Tyr
NM_001082959.1:c.1123C>T NP_001076428.1:p.His375Tyr
NM_005505.4:c.1123C>T NP_005496.4:p.His375Tyr
NM_005505.5:c.1123C>T MANE Select NP_005496.4:p.His375Tyr
NM_001082959.2:c.1123C>T NP_001076428.1:p.His375Tyr
NM_001367981.1:c.1123C>T NP_001354910.1:p.His375Tyr
NM_001367982.1:c.1000C>T NP_001354911.1:p.His334Tyr
NM_001367983.1:c.1123C>T NP_001354912.1:p.His375Tyr
NM_001367984.1:c.1123C>T NP_001354913.1:p.His375Tyr
NM_001367985.1:c.1099C>T NP_001354914.1:p.His367Tyr
NM_001367986.1:c.1123C>T NP_001354915.1:p.His375Tyr
NM_001367987.1:c.1004+7637C>T NP_001354916.1:n.1004+7637C>T
NM_001367988.1:c.727-4861C>T NP_001354917.1:n.727-4861C>T
NM_001367989.1:c.1123C>T NP_001354918.1:p.His375Tyr
NR_160416.1:n.1267C>T
NR_160417.1:n.1267C>T
NR_160418.1:n.1037+7632C>T
NR_160419.1:n.1267C>T
NR_160420.1:n.1151C>T
NR_160421.1:n.1153+7632C>T
NR_160422.1:n.1151C>T
NR_160423.1:n.1154-4861C>T
NR_160424.1:n.1262C>T