Canonical Allele Identifier: CA233492095

Gene: SLCO1C1

Linked Data

• dbSNP Id: rs1047504476
• MyVariant Identifiers: chr12:g.20860151_20860153del (hg19) ; chr12:g.20707217_20707219del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20707219_20707221del , CM000674.2:g.20707219_20707221del	GRCh38
NC_000012.11:g.20860153_20860155del , CM000674.1:g.20860153_20860155del	GRCh37
NC_000012.10:g.20751420_20751422del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266509.7:c.404+1138_404+1140del MANE Select	ENSP00000266509.2:n.404+1138_404+1140del
ENST00000266509.6:c.404+1138_404+1140del	ENSP00000266509.2:n.404+1138_404+1140del
ENST00000539415.5:c.130-4167_130-4165del	ENSP00000437399.1:n.130-4167_130-4165del
ENST00000540354.5:c.404+1138_404+1140del	ENSP00000438665.1:n.404+1138_404+1140del
ENST00000545102.1:c.50+1138_50+1140del	ENSP00000444527.1:n.50+1138_50+1140del
ENST00000545604.5:c.404+1138_404+1140del	ENSP00000444149.1:n.404+1138_404+1140del
NM_001145944.1:c.50+1138_50+1140del	NP_001139416.1:n.50+1138_50+1140del
NM_001145945.1:c.404+1138_404+1140del	NP_001139417.1:n.404+1138_404+1140del
NM_001145946.1:c.404+1138_404+1140del	NP_001139418.1:n.404+1138_404+1140del
NM_017435.4:c.404+1138_404+1140del	NP_059131.1:n.404+1138_404+1140del
XM_005253394.1:c.404+1138_404+1140del	XP_005253451.1:n.404+1138_404+1140del
XM_005253396.1:c.50+1138_50+1140del	XP_005253453.1:n.50+1138_50+1140del
XM_005253397.2:c.404+1138_404+1140del	XP_005253454.1:n.404+1138_404+1140del
XM_011520703.1:c.404+1138_404+1140del	XP_011519005.1:n.404+1138_404+1140del
XM_011520704.1:c.404+1138_404+1140del	XP_011519006.1:n.404+1138_404+1140del
XM_011520705.1:c.404+1138_404+1140del	XP_011519007.1:n.404+1138_404+1140del
XM_011520706.1:c.50+1138_50+1140del	XP_011519008.1:n.50+1138_50+1140del
XM_011520707.1:c.50+1138_50+1140del	XP_011519009.1:n.50+1138_50+1140del
XM_011520708.1:c.50+1138_50+1140del	XP_011519010.1:n.50+1138_50+1140del
XM_011520709.1:c.50+1138_50+1140del	XP_011519011.1:n.50+1138_50+1140del
XM_011520710.1:c.404+1138_404+1140del	XP_011519012.1:n.404+1138_404+1140del
XM_011520711.1:c.-150+1138_-150+1140del	XP_011519013.1:n.-150+1138_-150+1140del
XR_931308.1:n.759+1138_759+1140del
XM_005253394.3:c.404+1138_404+1140del	XP_005253451.1:n.404+1138_404+1140del
XM_005253396.3:c.50+1138_50+1140del	XP_005253453.1:n.50+1138_50+1140del
XM_011520703.3:c.404+1138_404+1140del	XP_011519005.1:n.404+1138_404+1140del
XM_011520704.3:c.404+1138_404+1140del	XP_011519006.1:n.404+1138_404+1140del
XM_011520711.3:c.-150+1138_-150+1140del	XP_011519013.1:n.-150+1138_-150+1140del
XM_017019486.2:c.50+1138_50+1140del	XP_016874975.1:n.50+1138_50+1140del
XM_017019487.2:c.50+1138_50+1140del	XP_016874976.1:n.50+1138_50+1140del
XM_017019489.2:c.-307+1138_-307+1140del	XP_016874978.1:n.-307+1138_-307+1140del
XM_017019490.2:c.-271+1138_-271+1140del	XP_016874979.1:n.-271+1138_-271+1140del
XM_024449024.1:c.50+1138_50+1140del	XP_024304792.1:n.50+1138_50+1140del
XM_024449025.1:c.50+1138_50+1140del	XP_024304793.1:n.50+1138_50+1140del
XR_001748768.2:n.13817+1138_13817+1140del
XR_001748769.2:n.13817+1138_13817+1140del
XR_001748770.2:n.13817+1138_13817+1140del
XR_001748771.2:n.14314+1138_14314+1140del
NM_001145944.2:c.50+1138_50+1140del	NP_001139416.1:n.50+1138_50+1140del
NM_001145945.2:c.404+1138_404+1140del	NP_001139417.1:n.404+1138_404+1140del
NM_001145946.2:c.404+1138_404+1140del	NP_001139418.1:n.404+1138_404+1140del
NM_017435.5:c.404+1138_404+1140del MANE Select	NP_059131.1:n.404+1138_404+1140del