Canonical Allele Identifier: CA2674746485
Gene: SLCO6A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102391089del , CM000667.2:g.102391089del GRCh38
NC_000005.9:g.101726793del , CM000667.1:g.101726793del GRCh37
NC_000005.8:g.101754692del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506729.6:c.1815-43del MANE Select ENSP00000421339.1:n.1815-43del
ENST00000379807.7:c.1815-43del ENSP00000369135.3:n.1815-43del
ENST00000389019.7:c.1629-43del ENSP00000373671.3:n.1629-43del
ENST00000506729.5:c.1815-43del ENSP00000421339.1:n.1815-43del
ENST00000513675.1:c.1056-43del ENSP00000421990.1:n.1056-43del
ENST00000514765.6:n.142del
NM_001289002.1:c.1815-43del NP_001275931.1:n.1815-43del
NM_001289004.1:c.1629-43del NP_001275933.1:n.1629-43del
NM_001308014.1:c.1056-43del NP_001294943.1:n.1056-43del
NM_173488.4:c.1815-43del NP_775759.3:n.1815-43del
XM_005271874.2:c.1815-43del XP_005271931.1:n.1815-43del
XM_011543147.1:c.1710-43del XP_011541449.1:n.1710-43del
XM_011543148.1:c.1578-43del XP_011541450.1:n.1578-43del
XM_011543149.1:c.1242-43del XP_011541451.1:n.1242-43del
XM_011543150.1:c.1086-43del XP_011541452.1:n.1086-43del
XM_011543151.1:c.1056-43del XP_011541453.1:n.1056-43del
XM_011543153.1:c.993-43del XP_011541455.1:n.993-43del
XM_005271874.3:c.1815-43del XP_005271931.1:n.1815-43del
XM_011543147.2:c.1710-43del XP_011541449.1:n.1710-43del
XM_011543148.2:c.1578-43del XP_011541450.1:n.1578-43del
XM_011543153.2:c.993-43del XP_011541455.1:n.993-43del
NM_001289002.2:c.1815-43del NP_001275931.1:n.1815-43del
NM_001289004.2:c.1629-43del NP_001275933.1:n.1629-43del
NM_001308014.2:c.1056-43del NP_001294943.1:n.1056-43del
NM_173488.5:c.1815-43del MANE Select NP_775759.3:n.1815-43del