Canonical Allele Identifier: CA2020746989

Gene: SLCO1C1

Linked Data

• dbSNP Id: rs1404607900

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20706778_20706779insCT , CM000674.2:g.20706778_20706779insCT	GRCh38
NC_000012.11:g.20859712_20859713insCT , CM000674.1:g.20859712_20859713insCT	GRCh37
NC_000012.10:g.20750979_20750980insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266509.7:c.404+697_404+698insCT MANE Select	ENSP00000266509.2:n.404+697_404+698insCT
ENST00000266509.6:c.404+697_404+698insCT	ENSP00000266509.2:n.404+697_404+698insCT
ENST00000539415.5:c.130-4608_130-4607insCT	ENSP00000437399.1:n.130-4608_130-4607insCT
ENST00000540354.5:c.404+697_404+698insCT	ENSP00000438665.1:n.404+697_404+698insCT
ENST00000545102.1:c.50+697_50+698insCT	ENSP00000444527.1:n.50+697_50+698insCT
ENST00000545604.5:c.404+697_404+698insCT	ENSP00000444149.1:n.404+697_404+698insCT
NM_001145944.1:c.50+697_50+698insCT	NP_001139416.1:n.50+697_50+698insCT
NM_001145945.1:c.404+697_404+698insCT	NP_001139417.1:n.404+697_404+698insCT
NM_001145946.1:c.404+697_404+698insCT	NP_001139418.1:n.404+697_404+698insCT
NM_017435.4:c.404+697_404+698insCT	NP_059131.1:n.404+697_404+698insCT
XM_005253394.1:c.404+697_404+698insCT	XP_005253451.1:n.404+697_404+698insCT
XM_005253396.1:c.50+697_50+698insCT	XP_005253453.1:n.50+697_50+698insCT
XM_005253397.2:c.404+697_404+698insCT	XP_005253454.1:n.404+697_404+698insCT
XM_011520703.1:c.404+697_404+698insCT	XP_011519005.1:n.404+697_404+698insCT
XM_011520704.1:c.404+697_404+698insCT	XP_011519006.1:n.404+697_404+698insCT
XM_011520705.1:c.404+697_404+698insCT	XP_011519007.1:n.404+697_404+698insCT
XM_011520706.1:c.50+697_50+698insCT	XP_011519008.1:n.50+697_50+698insCT
XM_011520707.1:c.50+697_50+698insCT	XP_011519009.1:n.50+697_50+698insCT
XM_011520708.1:c.50+697_50+698insCT	XP_011519010.1:n.50+697_50+698insCT
XM_011520709.1:c.50+697_50+698insCT	XP_011519011.1:n.50+697_50+698insCT
XM_011520710.1:c.404+697_404+698insCT	XP_011519012.1:n.404+697_404+698insCT
XM_011520711.1:c.-150+697_-150+698insCT	XP_011519013.1:n.-150+697_-150+698insCT
XR_931308.1:n.759+697_759+698insCT
XM_005253394.3:c.404+697_404+698insCT	XP_005253451.1:n.404+697_404+698insCT
XM_005253396.3:c.50+697_50+698insCT	XP_005253453.1:n.50+697_50+698insCT
XM_011520703.3:c.404+697_404+698insCT	XP_011519005.1:n.404+697_404+698insCT
XM_011520704.3:c.404+697_404+698insCT	XP_011519006.1:n.404+697_404+698insCT
XM_011520711.3:c.-150+697_-150+698insCT	XP_011519013.1:n.-150+697_-150+698insCT
XM_017019486.2:c.50+697_50+698insCT	XP_016874975.1:n.50+697_50+698insCT
XM_017019487.2:c.50+697_50+698insCT	XP_016874976.1:n.50+697_50+698insCT
XM_017019489.2:c.-307+697_-307+698insCT	XP_016874978.1:n.-307+697_-307+698insCT
XM_017019490.2:c.-271+697_-271+698insCT	XP_016874979.1:n.-271+697_-271+698insCT
XM_024449024.1:c.50+697_50+698insCT	XP_024304792.1:n.50+697_50+698insCT
XM_024449025.1:c.50+697_50+698insCT	XP_024304793.1:n.50+697_50+698insCT
XR_001748768.2:n.13817+697_13817+698insCT
XR_001748769.2:n.13817+697_13817+698insCT
XR_001748770.2:n.13817+697_13817+698insCT
XR_001748771.2:n.14314+697_14314+698insCT
NM_001145944.2:c.50+697_50+698insCT	NP_001139416.1:n.50+697_50+698insCT
NM_001145945.2:c.404+697_404+698insCT	NP_001139417.1:n.404+697_404+698insCT
NM_001145946.2:c.404+697_404+698insCT	NP_001139418.1:n.404+697_404+698insCT
NM_017435.5:c.404+697_404+698insCT MANE Select	NP_059131.1:n.404+697_404+698insCT