Canonical Allele Identifier: CA2674746435

Gene: SLCO6A1

Linked Data

• gnomAD v4: 5-102390912-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390912_102390913insG , CM000667.2:g.102390912_102390913insG	GRCh38
NC_000005.9:g.101726616_101726617insG , CM000667.1:g.101726616_101726617insG	GRCh37
NC_000005.8:g.101754515_101754516insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1879+68_1879+69insC MANE Select	ENSP00000421339.1:n.1879+68_1879+69insC
ENST00000379807.7:c.1879+68_1879+69insC	ENSP00000369135.3:n.1879+68_1879+69insC
ENST00000389019.7:c.1693+68_1693+69insC	ENSP00000373671.3:n.1693+68_1693+69insC
ENST00000506729.5:c.1879+68_1879+69insC	ENSP00000421339.1:n.1879+68_1879+69insC
ENST00000513675.1:c.1120+68_1120+69insC	ENSP00000421990.1:n.1120+68_1120+69insC
ENST00000514765.6:n.249+68_249+69insC
NM_001289002.1:c.1879+68_1879+69insC	NP_001275931.1:n.1879+68_1879+69insC
NM_001289004.1:c.1693+68_1693+69insC	NP_001275933.1:n.1693+68_1693+69insC
NM_001308014.1:c.1120+68_1120+69insC	NP_001294943.1:n.1120+68_1120+69insC
NM_173488.4:c.1879+68_1879+69insC	NP_775759.3:n.1879+68_1879+69insC
XM_005271874.2:c.1879+68_1879+69insC	XP_005271931.1:n.1879+68_1879+69insC
XM_011543147.1:c.1774+68_1774+69insC	XP_011541449.1:n.1774+68_1774+69insC
XM_011543148.1:c.1642+68_1642+69insC	XP_011541450.1:n.1642+68_1642+69insC
XM_011543149.1:c.1306+68_1306+69insC	XP_011541451.1:n.1306+68_1306+69insC
XM_011543150.1:c.1150+68_1150+69insC	XP_011541452.1:n.1150+68_1150+69insC
XM_011543151.1:c.1120+68_1120+69insC	XP_011541453.1:n.1120+68_1120+69insC
XM_011543153.1:c.1057+68_1057+69insC	XP_011541455.1:n.1057+68_1057+69insC
XM_005271874.3:c.1879+68_1879+69insC	XP_005271931.1:n.1879+68_1879+69insC
XM_011543147.2:c.1774+68_1774+69insC	XP_011541449.1:n.1774+68_1774+69insC
XM_011543148.2:c.1642+68_1642+69insC	XP_011541450.1:n.1642+68_1642+69insC
XM_011543153.2:c.1057+68_1057+69insC	XP_011541455.1:n.1057+68_1057+69insC
NM_001289002.2:c.1879+68_1879+69insC	NP_001275931.1:n.1879+68_1879+69insC
NM_001289004.2:c.1693+68_1693+69insC	NP_001275933.1:n.1693+68_1693+69insC
NM_001308014.2:c.1120+68_1120+69insC	NP_001294943.1:n.1120+68_1120+69insC
NM_173488.5:c.1879+68_1879+69insC MANE Select	NP_775759.3:n.1879+68_1879+69insC