Canonical Allele Identifier: CA1568270739

Gene: SLCO6A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390933_102390934delinsAT , CM000667.2:g.102390933_102390934delinsAT	GRCh38
NC_000005.9:g.101726637_101726638delinsAT , CM000667.1:g.101726637_101726638delinsAT	GRCh37
NC_000005.8:g.101754536_101754537delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1879+47_1879+48delinsAT MANE Select	ENSP00000421339.1:n.1879+47_1879+48delinsAT
ENST00000379807.7:c.1879+47_1879+48delinsAT	ENSP00000369135.3:n.1879+47_1879+48delinsAT
ENST00000389019.7:c.1693+47_1693+48delinsAT	ENSP00000373671.3:n.1693+47_1693+48delinsAT
ENST00000506729.5:c.1879+47_1879+48delinsAT	ENSP00000421339.1:n.1879+47_1879+48delinsAT
ENST00000513675.1:c.1120+47_1120+48delinsAT	ENSP00000421990.1:n.1120+47_1120+48delinsAT
ENST00000514765.6:n.249+47_249+48delinsAT
NM_001289002.1:c.1879+47_1879+48delinsAT	NP_001275931.1:n.1879+47_1879+48delinsAT
NM_001289004.1:c.1693+47_1693+48delinsAT	NP_001275933.1:n.1693+47_1693+48delinsAT
NM_001308014.1:c.1120+47_1120+48delinsAT	NP_001294943.1:n.1120+47_1120+48delinsAT
NM_173488.4:c.1879+47_1879+48delinsAT	NP_775759.3:n.1879+47_1879+48delinsAT
XM_005271874.2:c.1879+47_1879+48delinsAT	XP_005271931.1:n.1879+47_1879+48delinsAT
XM_011543147.1:c.1774+47_1774+48delinsAT	XP_011541449.1:n.1774+47_1774+48delinsAT
XM_011543148.1:c.1642+47_1642+48delinsAT	XP_011541450.1:n.1642+47_1642+48delinsAT
XM_011543149.1:c.1306+47_1306+48delinsAT	XP_011541451.1:n.1306+47_1306+48delinsAT
XM_011543150.1:c.1150+47_1150+48delinsAT	XP_011541452.1:n.1150+47_1150+48delinsAT
XM_011543151.1:c.1120+47_1120+48delinsAT	XP_011541453.1:n.1120+47_1120+48delinsAT
XM_011543153.1:c.1057+47_1057+48delinsAT	XP_011541455.1:n.1057+47_1057+48delinsAT
XM_005271874.3:c.1879+47_1879+48delinsAT	XP_005271931.1:n.1879+47_1879+48delinsAT
XM_011543147.2:c.1774+47_1774+48delinsAT	XP_011541449.1:n.1774+47_1774+48delinsAT
XM_011543148.2:c.1642+47_1642+48delinsAT	XP_011541450.1:n.1642+47_1642+48delinsAT
XM_011543153.2:c.1057+47_1057+48delinsAT	XP_011541455.1:n.1057+47_1057+48delinsAT
NM_001289002.2:c.1879+47_1879+48delinsAT	NP_001275931.1:n.1879+47_1879+48delinsAT
NM_001289004.2:c.1693+47_1693+48delinsAT	NP_001275933.1:n.1693+47_1693+48delinsAT
NM_001308014.2:c.1120+47_1120+48delinsAT	NP_001294943.1:n.1120+47_1120+48delinsAT
NM_173488.5:c.1879+47_1879+48delinsAT MANE Select	NP_775759.3:n.1879+47_1879+48delinsAT