Canonical Allele Identifier: CA2578371577

Gene: SLCO6A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390966G>A , CM000667.2:g.102390966G>A	GRCh38
NC_000005.9:g.101726670G>A , CM000667.1:g.101726670G>A	GRCh37
NC_000005.8:g.101754569G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506729.6:c.1879+15C>T MANE Select	ENSP00000421339.1:n.1879+15C>T
ENST00000379807.7:c.1879+15C>T	ENSP00000369135.3:n.1879+15C>T
ENST00000389019.7:c.1693+15C>T	ENSP00000373671.3:n.1693+15C>T
ENST00000506729.5:c.1879+15C>T	ENSP00000421339.1:n.1879+15C>T
ENST00000513675.1:c.1120+15C>T	ENSP00000421990.1:n.1120+15C>T
ENST00000514765.6:n.249+15C>T
NM_001289002.1:c.1879+15C>T	NP_001275931.1:n.1879+15C>T
NM_001289004.1:c.1693+15C>T	NP_001275933.1:n.1693+15C>T
NM_001308014.1:c.1120+15C>T	NP_001294943.1:n.1120+15C>T
NM_173488.4:c.1879+15C>T	NP_775759.3:n.1879+15C>T
XM_005271874.2:c.1879+15C>T	XP_005271931.1:n.1879+15C>T
XM_011543147.1:c.1774+15C>T	XP_011541449.1:n.1774+15C>T
XM_011543148.1:c.1642+15C>T	XP_011541450.1:n.1642+15C>T
XM_011543149.1:c.1306+15C>T	XP_011541451.1:n.1306+15C>T
XM_011543150.1:c.1150+15C>T	XP_011541452.1:n.1150+15C>T
XM_011543151.1:c.1120+15C>T	XP_011541453.1:n.1120+15C>T
XM_011543153.1:c.1057+15C>T	XP_011541455.1:n.1057+15C>T
XM_005271874.3:c.1879+15C>T	XP_005271931.1:n.1879+15C>T
XM_011543147.2:c.1774+15C>T	XP_011541449.1:n.1774+15C>T
XM_011543148.2:c.1642+15C>T	XP_011541450.1:n.1642+15C>T
XM_011543153.2:c.1057+15C>T	XP_011541455.1:n.1057+15C>T
NM_001289002.2:c.1879+15C>T	NP_001275931.1:n.1879+15C>T
NM_001289004.2:c.1693+15C>T	NP_001275933.1:n.1693+15C>T
NM_001308014.2:c.1120+15C>T	NP_001294943.1:n.1120+15C>T
NM_173488.5:c.1879+15C>T MANE Select	NP_775759.3:n.1879+15C>T