Canonical Allele Identifier: CA2674746446

Gene: SLCO6A1

Linked Data

• gnomAD v4: 5-102390923-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390925_102390926insGCA , CM000667.2:g.102390925_102390926insGCA	GRCh38
NC_000005.9:g.101726629_101726630insGCA , CM000667.1:g.101726629_101726630insGCA	GRCh37
NC_000005.8:g.101754528_101754529insGCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1879+57_1879+58insCTG MANE Select	ENSP00000421339.1:n.1879+57_1879+58insCTG
ENST00000379807.7:c.1879+57_1879+58insCTG	ENSP00000369135.3:n.1879+57_1879+58insCTG
ENST00000389019.7:c.1693+57_1693+58insCTG	ENSP00000373671.3:n.1693+57_1693+58insCTG
ENST00000506729.5:c.1879+57_1879+58insCTG	ENSP00000421339.1:n.1879+57_1879+58insCTG
ENST00000513675.1:c.1120+57_1120+58insCTG	ENSP00000421990.1:n.1120+57_1120+58insCTG
ENST00000514765.6:n.249+57_249+58insCTG
NM_001289002.1:c.1879+57_1879+58insCTG	NP_001275931.1:n.1879+57_1879+58insCTG
NM_001289004.1:c.1693+57_1693+58insCTG	NP_001275933.1:n.1693+57_1693+58insCTG
NM_001308014.1:c.1120+57_1120+58insCTG	NP_001294943.1:n.1120+57_1120+58insCTG
NM_173488.4:c.1879+57_1879+58insCTG	NP_775759.3:n.1879+57_1879+58insCTG
XM_005271874.2:c.1879+57_1879+58insCTG	XP_005271931.1:n.1879+57_1879+58insCTG
XM_011543147.1:c.1774+57_1774+58insCTG	XP_011541449.1:n.1774+57_1774+58insCTG
XM_011543148.1:c.1642+57_1642+58insCTG	XP_011541450.1:n.1642+57_1642+58insCTG
XM_011543149.1:c.1306+57_1306+58insCTG	XP_011541451.1:n.1306+57_1306+58insCTG
XM_011543150.1:c.1150+57_1150+58insCTG	XP_011541452.1:n.1150+57_1150+58insCTG
XM_011543151.1:c.1120+57_1120+58insCTG	XP_011541453.1:n.1120+57_1120+58insCTG
XM_011543153.1:c.1057+57_1057+58insCTG	XP_011541455.1:n.1057+57_1057+58insCTG
XM_005271874.3:c.1879+57_1879+58insCTG	XP_005271931.1:n.1879+57_1879+58insCTG
XM_011543147.2:c.1774+57_1774+58insCTG	XP_011541449.1:n.1774+57_1774+58insCTG
XM_011543148.2:c.1642+57_1642+58insCTG	XP_011541450.1:n.1642+57_1642+58insCTG
XM_011543153.2:c.1057+57_1057+58insCTG	XP_011541455.1:n.1057+57_1057+58insCTG
NM_001289002.2:c.1879+57_1879+58insCTG	NP_001275931.1:n.1879+57_1879+58insCTG
NM_001289004.2:c.1693+57_1693+58insCTG	NP_001275933.1:n.1693+57_1693+58insCTG
NM_001308014.2:c.1120+57_1120+58insCTG	NP_001294943.1:n.1120+57_1120+58insCTG
NM_173488.5:c.1879+57_1879+58insCTG MANE Select	NP_775759.3:n.1879+57_1879+58insCTG