Canonical Allele Identifier: CA2709617495
Gene: SLCO6A1 HGNC NCBI

Linked Data

dbSNP Id: rs2112522259

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102391455dup , CM000667.2:g.102391455dup GRCh38
NC_000005.9:g.101727159dup , CM000667.1:g.101727159dup GRCh37
NC_000005.8:g.101755058dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506729.6:c.1815-410dup MANE Select ENSP00000421339.1:n.1815-410dup
ENST00000379807.7:c.1815-410dup ENSP00000369135.3:n.1815-410dup
ENST00000389019.7:c.1629-410dup ENSP00000373671.3:n.1629-410dup
ENST00000506729.5:c.1815-410dup ENSP00000421339.1:n.1815-410dup
ENST00000513675.1:c.1056-410dup ENSP00000421990.1:n.1056-410dup
NM_001289002.1:c.1815-410dup NP_001275931.1:n.1815-410dup
NM_001289004.1:c.1629-410dup NP_001275933.1:n.1629-410dup
NM_001308014.1:c.1056-410dup NP_001294943.1:n.1056-410dup
NM_173488.4:c.1815-410dup NP_775759.3:n.1815-410dup
XM_005271874.2:c.1815-410dup XP_005271931.1:n.1815-410dup
XM_011543147.1:c.1710-410dup XP_011541449.1:n.1710-410dup
XM_011543148.1:c.1578-410dup XP_011541450.1:n.1578-410dup
XM_011543149.1:c.1242-410dup XP_011541451.1:n.1242-410dup
XM_011543150.1:c.1086-410dup XP_011541452.1:n.1086-410dup
XM_011543151.1:c.1056-410dup XP_011541453.1:n.1056-410dup
XM_011543153.1:c.993-410dup XP_011541455.1:n.993-410dup
XM_005271874.3:c.1815-410dup XP_005271931.1:n.1815-410dup
XM_011543147.2:c.1710-410dup XP_011541449.1:n.1710-410dup
XM_011543148.2:c.1578-410dup XP_011541450.1:n.1578-410dup
XM_011543153.2:c.993-410dup XP_011541455.1:n.993-410dup
NM_001289002.2:c.1815-410dup NP_001275931.1:n.1815-410dup
NM_001289004.2:c.1629-410dup NP_001275933.1:n.1629-410dup
NM_001308014.2:c.1056-410dup NP_001294943.1:n.1056-410dup
NM_173488.5:c.1815-410dup MANE Select NP_775759.3:n.1815-410dup