Canonical Allele Identifier: CA2645307035

Gene: SLC6A9

Linked Data

• gnomAD v4: 1-44000721-GGCCAAGGGGCAGCGGGGGAAGGGAGGGGCCGGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44000722_44000755del , CM000663.2:g.44000722_44000755del	GRCh38
NC_000001.10:g.44466394_44466427del , CM000663.1:g.44466394_44466427del	GRCh37
NC_000001.9:g.44238981_44239014del	NCBI36
NG_050929.1:g.35738_35771del

Transcript Alleles

HGVS	Amino-acid change
ENST00000372310.8:c.1536+12_1536+45del MANE Select	ENSP00000361384.4:n.1536+12_1536+45del
ENST00000673836.1:c.1536+12_1536+45del	ENSP00000501314.1:n.1536+12_1536+45del
ENST00000357730.6:c.1593+12_1593+45del	ENSP00000350362.2:n.1593+12_1593+45del
ENST00000360584.6:c.1755+12_1755+45del	ENSP00000353791.2:n.1755+12_1755+45del
ENST00000372306.7:c.1624+12_1624+45del	ENSP00000361380.3:n.1624+12_1624+45del
ENST00000372307.7:c.1341+12_1341+45del	ENSP00000361381.3:n.1341+12_1341+45del
ENST00000372310.7:c.1536+12_1536+45del	ENSP00000361384.3:n.1536+12_1536+45del
ENST00000475075.6:c.1203+12_1203+45del	ENSP00000434460.1:n.1203+12_1203+45del
NM_001024845.2:c.1536+12_1536+45del	NP_001020016.1:n.1536+12_1536+45del
NM_001261380.1:c.1548+12_1548+45del	NP_001248309.1:n.1548+12_1548+45del
NM_006934.3:c.1593+12_1593+45del	NP_008865.2:n.1593+12_1593+45del
NM_201649.3:c.1755+12_1755+45del	NP_964012.2:n.1755+12_1755+45del
NR_048548.1:n.1796+12_1796+45del
NR_048549.1:n.1519+12_1519+45del
XM_011542017.1:c.1755+12_1755+45del	XP_011540319.1:n.1755+12_1755+45del
NM_001328626.1:c.1203+12_1203+45del	NP_001315555.1:n.1203+12_1203+45del
NM_001328627.1:c.1473+12_1473+45del	NP_001315556.1:n.1473+12_1473+45del
NM_001328628.1:c.1341+12_1341+45del	NP_001315557.1:n.1341+12_1341+45del
NM_001328629.1:c.1536+12_1536+45del	NP_001315558.1:n.1536+12_1536+45del
NM_001328630.1:c.1203+12_1203+45del	NP_001315559.1:n.1203+12_1203+45del
XM_011542017.2:c.1755+12_1755+45del	XP_011540319.1:n.1755+12_1755+45del
XM_017002152.2:c.1455+12_1455+45del	XP_016857641.1:n.1455+12_1455+45del
XM_017002153.2:c.1422+12_1422+45del	XP_016857642.1:n.1422+12_1422+45del
XM_024449295.1:c.1341+12_1341+45del	XP_024305063.1:n.1341+12_1341+45del
NM_001024845.3:c.1536+12_1536+45del MANE Select	NP_001020016.1:n.1536+12_1536+45del
NM_001261380.2:c.1548+12_1548+45del	NP_001248309.1:n.1548+12_1548+45del
NM_001328626.2:c.1203+12_1203+45del	NP_001315555.1:n.1203+12_1203+45del
NM_001328630.2:c.1203+12_1203+45del	NP_001315559.1:n.1203+12_1203+45del
NM_006934.4:c.1593+12_1593+45del	NP_008865.2:n.1593+12_1593+45del
NM_201649.4:c.1755+12_1755+45del	NP_964012.2:n.1755+12_1755+45del
NR_048548.2:n.1619+12_1619+45del