Canonical Allele Identifier: CA482281900

Gene: SCARB1

Linked Data

• MyVariant Identifiers: chr12:g.125284754G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124800208G>A , CM000674.2:g.124800208G>A	GRCh38
NC_000012.11:g.125284754G>A , CM000674.1:g.125284754G>A	GRCh37
NC_000012.10:g.123850707G>A	NCBI36
NG_028199.1:g.68766C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261693.11:c.1044C>T MANE Select	ENSP00000261693.6:p.Leu348=
ENST00000679605.1:c.*128+7553C>T	ENSP00000505370.1:n.*128+7553C>T
ENST00000679955.1:n.2768C>T
ENST00000680556.1:c.1004+7558C>T	ENSP00000505757.1:n.1004+7558C>T
ENST00000680596.1:c.1020C>T	ENSP00000505605.1:p.Leu340=
ENST00000680926.1:c.1039C>T	ENSP00000505571.1:p.Gln347Ter
ENST00000680982.1:c.*1027C>T	ENSP00000506281.1:n.*1027C>T
ENST00000681117.1:c.*163C>T	ENSP00000506693.1:n.*163C>T
ENST00000681499.1:n.917C>T
ENST00000681555.1:n.734C>T
ENST00000681686.1:c.1044C>T	ENSP00000505406.1:p.Leu348=
ENST00000261693.10:c.1044C>T	ENSP00000261693.6:p.Leu348=
ENST00000339570.9:c.1044C>T	ENSP00000343795.4:p.Leu348=
ENST00000415380.6:c.1044C>T	ENSP00000414979.2:p.Leu348=
ENST00000535005.5:n.1359C>T
ENST00000538291.5:n.1187C>T
ENST00000544327.1:c.882C>T	ENSP00000444851.1:p.Leu294=
ENST00000546215.5:c.1044C>T	ENSP00000442862.1:p.Leu348=
NM_001082959.1:c.1044C>T	NP_001076428.1:p.Leu348=
NM_005505.4:c.1044C>T	NP_005496.4:p.Leu348=
NM_005505.5:c.1044C>T MANE Select	NP_005496.4:p.Leu348=
NM_001082959.2:c.1044C>T	NP_001076428.1:p.Leu348=
NM_001367981.1:c.1044C>T	NP_001354910.1:p.Leu348=
NM_001367982.1:c.921C>T	NP_001354911.1:p.Leu307=
NM_001367983.1:c.1044C>T	NP_001354912.1:p.Leu348=
NM_001367984.1:c.1044C>T	NP_001354913.1:p.Leu348=
NM_001367985.1:c.1020C>T	NP_001354914.1:p.Leu340=
NM_001367986.1:c.1044C>T	NP_001354915.1:p.Leu348=
NM_001367987.1:c.1004+7558C>T	NP_001354916.1:n.1004+7558C>T
NM_001367988.1:c.727-4940C>T	NP_001354917.1:n.727-4940C>T
NM_001367989.1:c.1044C>T	NP_001354918.1:p.Leu348=
NR_160416.1:n.1188C>T
NR_160417.1:n.1188C>T
NR_160418.1:n.1037+7553C>T
NR_160419.1:n.1188C>T
NR_160420.1:n.1072C>T
NR_160421.1:n.1153+7553C>T
NR_160422.1:n.1072C>T
NR_160423.1:n.1154-4940C>T
NR_160424.1:n.1183C>T