Canonical Allele Identifier: CA2674746612
Gene: SLCO6A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102391213del , CM000667.2:g.102391213del GRCh38
NC_000005.9:g.101726917del , CM000667.1:g.101726917del GRCh37
NC_000005.8:g.101754816del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506729.6:c.1815-165del MANE Select ENSP00000421339.1:n.1815-165del
ENST00000379807.7:c.1815-165del ENSP00000369135.3:n.1815-165del
ENST00000389019.7:c.1629-165del ENSP00000373671.3:n.1629-165del
ENST00000506729.5:c.1815-165del ENSP00000421339.1:n.1815-165del
ENST00000513675.1:c.1056-165del ENSP00000421990.1:n.1056-165del
ENST00000514765.6:n.20del
NM_001289002.1:c.1815-165del NP_001275931.1:n.1815-165del
NM_001289004.1:c.1629-165del NP_001275933.1:n.1629-165del
NM_001308014.1:c.1056-165del NP_001294943.1:n.1056-165del
NM_173488.4:c.1815-165del NP_775759.3:n.1815-165del
XM_005271874.2:c.1815-165del XP_005271931.1:n.1815-165del
XM_011543147.1:c.1710-165del XP_011541449.1:n.1710-165del
XM_011543148.1:c.1578-165del XP_011541450.1:n.1578-165del
XM_011543149.1:c.1242-165del XP_011541451.1:n.1242-165del
XM_011543150.1:c.1086-165del XP_011541452.1:n.1086-165del
XM_011543151.1:c.1056-165del XP_011541453.1:n.1056-165del
XM_011543153.1:c.993-165del XP_011541455.1:n.993-165del
XM_005271874.3:c.1815-165del XP_005271931.1:n.1815-165del
XM_011543147.2:c.1710-165del XP_011541449.1:n.1710-165del
XM_011543148.2:c.1578-165del XP_011541450.1:n.1578-165del
XM_011543153.2:c.993-165del XP_011541455.1:n.993-165del
NM_001289002.2:c.1815-165del NP_001275931.1:n.1815-165del
NM_001289004.2:c.1629-165del NP_001275933.1:n.1629-165del
NM_001308014.2:c.1056-165del NP_001294943.1:n.1056-165del
NM_173488.5:c.1815-165del MANE Select NP_775759.3:n.1815-165del