Canonical Allele Identifier: CA2020747063
Gene: SLCO1C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20706934_20706935delinsCT , CM000674.2:g.20706934_20706935delinsCT GRCh38
NC_000012.11:g.20859868_20859869delinsCT , CM000674.1:g.20859868_20859869delinsCT GRCh37
NC_000012.10:g.20751135_20751136delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266509.7:c.404+853_404+854delinsCT MANE Select ENSP00000266509.2:n.404+853_404+854delinsCT
ENST00000266509.6:c.404+853_404+854delinsCT ENSP00000266509.2:n.404+853_404+854delinsCT
ENST00000539415.5:c.130-4452_130-4451delinsCT ENSP00000437399.1:n.130-4452_130-4451delinsCT
ENST00000540354.5:c.404+853_404+854delinsCT ENSP00000438665.1:n.404+853_404+854delinsCT
ENST00000545102.1:c.50+853_50+854delinsCT ENSP00000444527.1:n.50+853_50+854delinsCT
ENST00000545604.5:c.404+853_404+854delinsCT ENSP00000444149.1:n.404+853_404+854delinsCT
NM_001145944.1:c.50+853_50+854delinsCT NP_001139416.1:n.50+853_50+854delinsCT
NM_001145945.1:c.404+853_404+854delinsCT NP_001139417.1:n.404+853_404+854delinsCT
NM_001145946.1:c.404+853_404+854delinsCT NP_001139418.1:n.404+853_404+854delinsCT
NM_017435.4:c.404+853_404+854delinsCT NP_059131.1:n.404+853_404+854delinsCT
XM_005253394.1:c.404+853_404+854delinsCT XP_005253451.1:n.404+853_404+854delinsCT
XM_005253396.1:c.50+853_50+854delinsCT XP_005253453.1:n.50+853_50+854delinsCT
XM_005253397.2:c.404+853_404+854delinsCT XP_005253454.1:n.404+853_404+854delinsCT
XM_011520703.1:c.404+853_404+854delinsCT XP_011519005.1:n.404+853_404+854delinsCT
XM_011520704.1:c.404+853_404+854delinsCT XP_011519006.1:n.404+853_404+854delinsCT
XM_011520705.1:c.404+853_404+854delinsCT XP_011519007.1:n.404+853_404+854delinsCT
XM_011520706.1:c.50+853_50+854delinsCT XP_011519008.1:n.50+853_50+854delinsCT
XM_011520707.1:c.50+853_50+854delinsCT XP_011519009.1:n.50+853_50+854delinsCT
XM_011520708.1:c.50+853_50+854delinsCT XP_011519010.1:n.50+853_50+854delinsCT
XM_011520709.1:c.50+853_50+854delinsCT XP_011519011.1:n.50+853_50+854delinsCT
XM_011520710.1:c.404+853_404+854delinsCT XP_011519012.1:n.404+853_404+854delinsCT
XM_011520711.1:c.-150+853_-150+854delinsCT XP_011519013.1:n.-150+853_-150+854delinsCT
XR_931308.1:n.759+853_759+854delinsCT
XM_005253394.3:c.404+853_404+854delinsCT XP_005253451.1:n.404+853_404+854delinsCT
XM_005253396.3:c.50+853_50+854delinsCT XP_005253453.1:n.50+853_50+854delinsCT
XM_011520703.3:c.404+853_404+854delinsCT XP_011519005.1:n.404+853_404+854delinsCT
XM_011520704.3:c.404+853_404+854delinsCT XP_011519006.1:n.404+853_404+854delinsCT
XM_011520711.3:c.-150+853_-150+854delinsCT XP_011519013.1:n.-150+853_-150+854delinsCT
XM_017019486.2:c.50+853_50+854delinsCT XP_016874975.1:n.50+853_50+854delinsCT
XM_017019487.2:c.50+853_50+854delinsCT XP_016874976.1:n.50+853_50+854delinsCT
XM_017019489.2:c.-307+853_-307+854delinsCT XP_016874978.1:n.-307+853_-307+854delinsCT
XM_017019490.2:c.-271+853_-271+854delinsCT XP_016874979.1:n.-271+853_-271+854delinsCT
XM_024449024.1:c.50+853_50+854delinsCT XP_024304792.1:n.50+853_50+854delinsCT
XM_024449025.1:c.50+853_50+854delinsCT XP_024304793.1:n.50+853_50+854delinsCT
XR_001748768.2:n.13817+853_13817+854delinsCT
XR_001748769.2:n.13817+853_13817+854delinsCT
XR_001748770.2:n.13817+853_13817+854delinsCT
XR_001748771.2:n.14314+853_14314+854delinsCT
NM_001145944.2:c.50+853_50+854delinsCT NP_001139416.1:n.50+853_50+854delinsCT
NM_001145945.2:c.404+853_404+854delinsCT NP_001139417.1:n.404+853_404+854delinsCT
NM_001145946.2:c.404+853_404+854delinsCT NP_001139418.1:n.404+853_404+854delinsCT
NM_017435.5:c.404+853_404+854delinsCT MANE Select NP_059131.1:n.404+853_404+854delinsCT