Canonical Allele Identifier: CA2020745834

Gene: SLCO1C1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20704210_20704211delinsCT , CM000674.2:g.20704210_20704211delinsCT	GRCh38
NC_000012.11:g.20857144_20857145delinsCT , CM000674.1:g.20857144_20857145delinsCT	GRCh37
NC_000012.10:g.20748411_20748412delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266509.7:c.272-1739_272-1738delinsCT MANE Select	ENSP00000266509.2:n.272-1739_272-1738delinsCT
ENST00000266509.6:c.272-1739_272-1738delinsCT	ENSP00000266509.2:n.272-1739_272-1738delinsCT
ENST00000539415.5:c.129+4505_129+4506delinsCT	ENSP00000437399.1:n.129+4505_129+4506delinsCT
ENST00000540354.5:c.272-1739_272-1738delinsCT	ENSP00000438665.1:n.272-1739_272-1738delinsCT
ENST00000545102.1:c.-83-1739_-83-1738delinsCT	ENSP00000444527.1:n.-83-1739_-83-1738delinsCT
ENST00000545604.5:c.272-1739_272-1738delinsCT	ENSP00000444149.1:n.272-1739_272-1738delinsCT
NM_001145944.1:c.-83-1739_-83-1738delinsCT	NP_001139416.1:n.-83-1739_-83-1738delinsCT
NM_001145945.1:c.272-1739_272-1738delinsCT	NP_001139417.1:n.272-1739_272-1738delinsCT
NM_001145946.1:c.272-1739_272-1738delinsCT	NP_001139418.1:n.272-1739_272-1738delinsCT
NM_017435.4:c.272-1739_272-1738delinsCT	NP_059131.1:n.272-1739_272-1738delinsCT
XM_005253394.1:c.272-1739_272-1738delinsCT	XP_005253451.1:n.272-1739_272-1738delinsCT
XM_005253396.1:c.-83-1739_-83-1738delinsCT	XP_005253453.1:n.-83-1739_-83-1738delinsCT
XM_005253397.2:c.272-1739_272-1738delinsCT	XP_005253454.1:n.272-1739_272-1738delinsCT
XM_011520703.1:c.272-1739_272-1738delinsCT	XP_011519005.1:n.272-1739_272-1738delinsCT
XM_011520704.1:c.272-1739_272-1738delinsCT	XP_011519006.1:n.272-1739_272-1738delinsCT
XM_011520705.1:c.272-1739_272-1738delinsCT	XP_011519007.1:n.272-1739_272-1738delinsCT
XM_011520706.1:c.-84+1492_-84+1493delinsCT	XP_011519008.1:n.-84+1492_-84+1493delinsCT
XM_011520707.1:c.-83-1739_-83-1738delinsCT	XP_011519009.1:n.-83-1739_-83-1738delinsCT
XM_011520708.1:c.-83-1739_-83-1738delinsCT	XP_011519010.1:n.-83-1739_-83-1738delinsCT
XM_011520709.1:c.-83-1739_-83-1738delinsCT	XP_011519011.1:n.-83-1739_-83-1738delinsCT
XM_011520710.1:c.272-1739_272-1738delinsCT	XP_011519012.1:n.272-1739_272-1738delinsCT
XM_011520711.1:c.-282-1739_-282-1738delinsCT	XP_011519013.1:n.-282-1739_-282-1738delinsCT
XR_931308.1:n.627-1739_627-1738delinsCT
XM_005253394.3:c.272-1739_272-1738delinsCT	XP_005253451.1:n.272-1739_272-1738delinsCT
XM_005253396.3:c.-83-1739_-83-1738delinsCT	XP_005253453.1:n.-83-1739_-83-1738delinsCT
XM_011520703.3:c.272-1739_272-1738delinsCT	XP_011519005.1:n.272-1739_272-1738delinsCT
XM_011520704.3:c.272-1739_272-1738delinsCT	XP_011519006.1:n.272-1739_272-1738delinsCT
XM_011520711.3:c.-282-1739_-282-1738delinsCT	XP_011519013.1:n.-282-1739_-282-1738delinsCT
XM_017019486.2:c.-83-1739_-83-1738delinsCT	XP_016874975.1:n.-83-1739_-83-1738delinsCT
XM_017019487.2:c.-83-1739_-83-1738delinsCT	XP_016874976.1:n.-83-1739_-83-1738delinsCT
XM_017019489.2:c.-440+1492_-440+1493delinsCT	XP_016874978.1:n.-440+1492_-440+1493delinsCT
XM_017019490.2:c.-404+1492_-404+1493delinsCT	XP_016874979.1:n.-404+1492_-404+1493delinsCT
XM_024449024.1:c.-84+1492_-84+1493delinsCT	XP_024304792.1:n.-84+1492_-84+1493delinsCT
XM_024449025.1:c.-83-1739_-83-1738delinsCT	XP_024304793.1:n.-83-1739_-83-1738delinsCT
XR_001748768.2:n.13685-1739_13685-1738delinsCT
XR_001748769.2:n.13685-1739_13685-1738delinsCT
XR_001748770.2:n.13685-1739_13685-1738delinsCT
XR_001748771.2:n.14182-1739_14182-1738delinsCT
NM_001145944.2:c.-83-1739_-83-1738delinsCT	NP_001139416.1:n.-83-1739_-83-1738delinsCT
NM_001145945.2:c.272-1739_272-1738delinsCT	NP_001139417.1:n.272-1739_272-1738delinsCT
NM_001145946.2:c.272-1739_272-1738delinsCT	NP_001139418.1:n.272-1739_272-1738delinsCT
NM_017435.5:c.272-1739_272-1738delinsCT MANE Select	NP_059131.1:n.272-1739_272-1738delinsCT