Canonical Allele Identifier: CA2674746422

Gene: SLCO6A1

Linked Data

• gnomAD v4: 5-102390892-T-TACAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390893_102390894insCAAA , CM000667.2:g.102390893_102390894insCAAA	GRCh38
NC_000005.9:g.101726597_101726598insCAAA , CM000667.1:g.101726597_101726598insCAAA	GRCh37
NC_000005.8:g.101754496_101754497insCAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1879+88_1879+89insTTGT MANE Select	ENSP00000421339.1:n.1879+88_1879+89insTTGT
ENST00000379807.7:c.1879+88_1879+89insTTGT	ENSP00000369135.3:n.1879+88_1879+89insTTGT
ENST00000389019.7:c.1693+88_1693+89insTTGT	ENSP00000373671.3:n.1693+88_1693+89insTTGT
ENST00000506729.5:c.1879+88_1879+89insTTGT	ENSP00000421339.1:n.1879+88_1879+89insTTGT
ENST00000513675.1:c.1120+88_1120+89insTTGT	ENSP00000421990.1:n.1120+88_1120+89insTTGT
ENST00000514765.6:n.249+88_249+89insTTGT
NM_001289002.1:c.1879+88_1879+89insTTGT	NP_001275931.1:n.1879+88_1879+89insTTGT
NM_001289004.1:c.1693+88_1693+89insTTGT	NP_001275933.1:n.1693+88_1693+89insTTGT
NM_001308014.1:c.1120+88_1120+89insTTGT	NP_001294943.1:n.1120+88_1120+89insTTGT
NM_173488.4:c.1879+88_1879+89insTTGT	NP_775759.3:n.1879+88_1879+89insTTGT
XM_005271874.2:c.1879+88_1879+89insTTGT	XP_005271931.1:n.1879+88_1879+89insTTGT
XM_011543147.1:c.1774+88_1774+89insTTGT	XP_011541449.1:n.1774+88_1774+89insTTGT
XM_011543148.1:c.1642+88_1642+89insTTGT	XP_011541450.1:n.1642+88_1642+89insTTGT
XM_011543149.1:c.1306+88_1306+89insTTGT	XP_011541451.1:n.1306+88_1306+89insTTGT
XM_011543150.1:c.1150+88_1150+89insTTGT	XP_011541452.1:n.1150+88_1150+89insTTGT
XM_011543151.1:c.1120+88_1120+89insTTGT	XP_011541453.1:n.1120+88_1120+89insTTGT
XM_011543153.1:c.1057+88_1057+89insTTGT	XP_011541455.1:n.1057+88_1057+89insTTGT
XM_005271874.3:c.1879+88_1879+89insTTGT	XP_005271931.1:n.1879+88_1879+89insTTGT
XM_011543147.2:c.1774+88_1774+89insTTGT	XP_011541449.1:n.1774+88_1774+89insTTGT
XM_011543148.2:c.1642+88_1642+89insTTGT	XP_011541450.1:n.1642+88_1642+89insTTGT
XM_011543153.2:c.1057+88_1057+89insTTGT	XP_011541455.1:n.1057+88_1057+89insTTGT
NM_001289002.2:c.1879+88_1879+89insTTGT	NP_001275931.1:n.1879+88_1879+89insTTGT
NM_001289004.2:c.1693+88_1693+89insTTGT	NP_001275933.1:n.1693+88_1693+89insTTGT
NM_001308014.2:c.1120+88_1120+89insTTGT	NP_001294943.1:n.1120+88_1120+89insTTGT
NM_173488.5:c.1879+88_1879+89insTTGT MANE Select	NP_775759.3:n.1879+88_1879+89insTTGT