Canonical Allele Identifier: CA123847372
Gene: SLCO6A1 HGNC NCBI

Linked Data

dbSNP Id: rs34681516

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102391441dup , CM000667.2:g.102391441dup GRCh38
NC_000005.9:g.101727145dup , CM000667.1:g.101727145dup GRCh37
NC_000005.8:g.101755044dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506729.6:c.1815-394dup MANE Select ENSP00000421339.1:n.1815-394dup
ENST00000379807.7:c.1815-394dup ENSP00000369135.3:n.1815-394dup
ENST00000389019.7:c.1629-394dup ENSP00000373671.3:n.1629-394dup
ENST00000506729.5:c.1815-394dup ENSP00000421339.1:n.1815-394dup
ENST00000513675.1:c.1056-394dup ENSP00000421990.1:n.1056-394dup
NM_001289002.1:c.1815-394dup NP_001275931.1:n.1815-394dup
NM_001289004.1:c.1629-394dup NP_001275933.1:n.1629-394dup
NM_001308014.1:c.1056-394dup NP_001294943.1:n.1056-394dup
NM_173488.4:c.1815-394dup NP_775759.3:n.1815-394dup
XM_005271874.2:c.1815-394dup XP_005271931.1:n.1815-394dup
XM_011543147.1:c.1710-394dup XP_011541449.1:n.1710-394dup
XM_011543148.1:c.1578-394dup XP_011541450.1:n.1578-394dup
XM_011543149.1:c.1242-394dup XP_011541451.1:n.1242-394dup
XM_011543150.1:c.1086-394dup XP_011541452.1:n.1086-394dup
XM_011543151.1:c.1056-394dup XP_011541453.1:n.1056-394dup
XM_011543153.1:c.993-394dup XP_011541455.1:n.993-394dup
XM_005271874.3:c.1815-394dup XP_005271931.1:n.1815-394dup
XM_011543147.2:c.1710-394dup XP_011541449.1:n.1710-394dup
XM_011543148.2:c.1578-394dup XP_011541450.1:n.1578-394dup
XM_011543153.2:c.993-394dup XP_011541455.1:n.993-394dup
NM_001289002.2:c.1815-394dup NP_001275931.1:n.1815-394dup
NM_001289004.2:c.1629-394dup NP_001275933.1:n.1629-394dup
NM_001308014.2:c.1056-394dup NP_001294943.1:n.1056-394dup
NM_173488.5:c.1815-394dup MANE Select NP_775759.3:n.1815-394dup