Canonical Allele Identifier: CA13698782

Gene: SCARB1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124804719G>A , CM000674.2:g.124804719G>A	GRCh38
NC_000012.11:g.125289265G>A , CM000674.1:g.125289265G>A	GRCh37
NC_000012.10:g.123855218G>A	NCBI36
NG_028199.1:g.64255C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.1009+3042C>T MANE Select	ENSP00000261693.6:n.1009+3042C>T
ENST00000679605.1:c.*128+3042C>T	ENSP00000505370.1:n.*128+3042C>T
ENST00000680556.1:c.1004+3047C>T	ENSP00000505757.1:n.1004+3047C>T
ENST00000680596.1:c.985+3042C>T	ENSP00000505605.1:n.985+3042C>T
ENST00000680926.1:c.1004+3047C>T	ENSP00000505571.1:n.1004+3047C>T
ENST00000680982.1:c.*992+3042C>T	ENSP00000506281.1:n.*992+3042C>T
ENST00000681117.1:c.*128+3042C>T	ENSP00000506693.1:n.*128+3042C>T
ENST00000681499.1:n.882+3042C>T
ENST00000681555.1:n.699+3042C>T
ENST00000681686.1:c.1009+3042C>T	ENSP00000505406.1:n.1009+3042C>T
ENST00000261693.10:c.1009+3042C>T	ENSP00000261693.6:n.1009+3042C>T
ENST00000339570.9:c.1009+3042C>T	ENSP00000343795.4:n.1009+3042C>T
ENST00000415380.6:c.1009+3042C>T	ENSP00000414979.2:n.1009+3042C>T
ENST00000535005.5:n.1324+3042C>T
ENST00000538291.5:n.1152+3042C>T
ENST00000544327.1:c.847+3042C>T	ENSP00000444851.1:n.847+3042C>T
ENST00000546215.5:c.1009+3042C>T	ENSP00000442862.1:n.1009+3042C>T
NM_001082959.1:c.1009+3042C>T	NP_001076428.1:n.1009+3042C>T
NM_005505.4:c.1009+3042C>T	NP_005496.4:n.1009+3042C>T
NM_005505.5:c.1009+3042C>T MANE Select	NP_005496.4:n.1009+3042C>T
NM_001082959.2:c.1009+3042C>T	NP_001076428.1:n.1009+3042C>T
NM_001367981.1:c.1009+3042C>T	NP_001354910.1:n.1009+3042C>T
NM_001367982.1:c.886+3042C>T	NP_001354911.1:n.886+3042C>T
NM_001367983.1:c.1009+3042C>T	NP_001354912.1:n.1009+3042C>T
NM_001367984.1:c.1009+3042C>T	NP_001354913.1:n.1009+3042C>T
NM_001367985.1:c.985+3042C>T	NP_001354914.1:n.985+3042C>T
NM_001367986.1:c.1009+3042C>T	NP_001354915.1:n.1009+3042C>T
NM_001367987.1:c.1004+3047C>T	NP_001354916.1:n.1004+3047C>T
NM_001367988.1:c.726+7151C>T	NP_001354917.1:n.726+7151C>T
NM_001367989.1:c.1009+3042C>T	NP_001354918.1:n.1009+3042C>T
NR_160416.1:n.1153+3042C>T
NR_160417.1:n.1153+3042C>T
NR_160418.1:n.1037+3042C>T
NR_160419.1:n.1153+3042C>T
NR_160420.1:n.1037+3042C>T
NR_160421.1:n.1153+3042C>T
NR_160422.1:n.1037+3042C>T
NR_160423.1:n.1153+3042C>T
NR_160424.1:n.1148+3047C>T