Canonical Allele Identifier: CA945468050

Gene: SLCO1C1

Linked Data

• dbSNP Id: rs1946804845
• gnomAD v3: 12-20706866-T-TA
• gnomAD v4: 12-20706866-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20706870dup , CM000674.2:g.20706870dup	GRCh38
NC_000012.11:g.20859804dup , CM000674.1:g.20859804dup	GRCh37
NC_000012.10:g.20751071dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266509.7:c.404+789dup MANE Select	ENSP00000266509.2:n.404+789dup
ENST00000266509.6:c.404+789dup	ENSP00000266509.2:n.404+789dup
ENST00000539415.5:c.130-4516dup	ENSP00000437399.1:n.130-4516dup
ENST00000540354.5:c.404+789dup	ENSP00000438665.1:n.404+789dup
ENST00000545102.1:c.50+789dup	ENSP00000444527.1:n.50+789dup
ENST00000545604.5:c.404+789dup	ENSP00000444149.1:n.404+789dup
NM_001145944.1:c.50+789dup	NP_001139416.1:n.50+789dup
NM_001145945.1:c.404+789dup	NP_001139417.1:n.404+789dup
NM_001145946.1:c.404+789dup	NP_001139418.1:n.404+789dup
NM_017435.4:c.404+789dup	NP_059131.1:n.404+789dup
XM_005253394.1:c.404+789dup	XP_005253451.1:n.404+789dup
XM_005253396.1:c.50+789dup	XP_005253453.1:n.50+789dup
XM_005253397.2:c.404+789dup	XP_005253454.1:n.404+789dup
XM_011520703.1:c.404+789dup	XP_011519005.1:n.404+789dup
XM_011520704.1:c.404+789dup	XP_011519006.1:n.404+789dup
XM_011520705.1:c.404+789dup	XP_011519007.1:n.404+789dup
XM_011520706.1:c.50+789dup	XP_011519008.1:n.50+789dup
XM_011520707.1:c.50+789dup	XP_011519009.1:n.50+789dup
XM_011520708.1:c.50+789dup	XP_011519010.1:n.50+789dup
XM_011520709.1:c.50+789dup	XP_011519011.1:n.50+789dup
XM_011520710.1:c.404+789dup	XP_011519012.1:n.404+789dup
XM_011520711.1:c.-150+789dup	XP_011519013.1:n.-150+789dup
XR_931308.1:n.759+789dup
XM_005253394.3:c.404+789dup	XP_005253451.1:n.404+789dup
XM_005253396.3:c.50+789dup	XP_005253453.1:n.50+789dup
XM_011520703.3:c.404+789dup	XP_011519005.1:n.404+789dup
XM_011520704.3:c.404+789dup	XP_011519006.1:n.404+789dup
XM_011520711.3:c.-150+789dup	XP_011519013.1:n.-150+789dup
XM_017019486.2:c.50+789dup	XP_016874975.1:n.50+789dup
XM_017019487.2:c.50+789dup	XP_016874976.1:n.50+789dup
XM_017019489.2:c.-307+789dup	XP_016874978.1:n.-307+789dup
XM_017019490.2:c.-271+789dup	XP_016874979.1:n.-271+789dup
XM_024449024.1:c.50+789dup	XP_024304792.1:n.50+789dup
XM_024449025.1:c.50+789dup	XP_024304793.1:n.50+789dup
XR_001748768.2:n.13817+789dup
XR_001748769.2:n.13817+789dup
XR_001748770.2:n.13817+789dup
XR_001748771.2:n.14314+789dup
NM_001145944.2:c.50+789dup	NP_001139416.1:n.50+789dup
NM_001145945.2:c.404+789dup	NP_001139417.1:n.404+789dup
NM_001145946.2:c.404+789dup	NP_001139418.1:n.404+789dup
NM_017435.5:c.404+789dup MANE Select	NP_059131.1:n.404+789dup