Canonical Allele Identifier: CA2841462564

Gene: SLC6A9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44001504dup , CM000663.2:g.44001504dup	GRCh38
NC_000001.10:g.44467176dup , CM000663.1:g.44467176dup	GRCh37
NC_000001.9:g.44239763dup	NCBI36
NG_050929.1:g.34989dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372310.8:c.1086dup MANE Select	ENSP00000361384.4:p.Gly363ArgfsTer?
ENST00000673836.1:c.1086dup	ENSP00000501314.1:p.Gly363ArgfsTer?
ENST00000357730.6:c.1143dup	ENSP00000350362.2:p.Gly382ArgfsTer?
ENST00000360584.6:c.1305dup	ENSP00000353791.2:p.Gly436ArgfsTer?
ENST00000372306.7:c.1086dup	ENSP00000361380.3:p.Gly363ArgfsTer?
ENST00000372307.7:c.891dup	ENSP00000361381.3:p.Gly298ArgfsTer?
ENST00000372310.7:c.1086dup	ENSP00000361384.3:p.Gly363ArgfsTer?
ENST00000475075.6:c.753dup	ENSP00000434460.1:p.Gly252ArgfsTer?
NM_001024845.2:c.1086dup	NP_001020016.1:p.Gly363ArgfsTer?
NM_001261380.1:c.1098dup	NP_001248309.1:p.Gly367ArgfsTer?
NM_006934.3:c.1143dup	NP_008865.2:p.Gly382ArgfsTer?
NM_201649.3:c.1305dup	NP_964012.2:p.Gly436ArgfsTer?
NR_048548.1:n.1350dup
NR_048549.1:n.1069dup
XM_011542017.1:c.1305dup	XP_011540319.1:p.Gly436ArgfsTer?
NM_001328626.1:c.753dup	NP_001315555.1:p.Gly252ArgfsTer?
NM_001328627.1:c.1023dup	NP_001315556.1:p.Gly342ArgfsTer?
NM_001328628.1:c.891dup	NP_001315557.1:p.Gly298ArgfsTer?
NM_001328629.1:c.1086dup	NP_001315558.1:p.Gly363ArgfsTer?
NM_001328630.1:c.753dup	NP_001315559.1:p.Gly252ArgfsTer?
XM_011542017.2:c.1305dup	XP_011540319.1:p.Gly436ArgfsTer?
XM_017002152.2:c.1005dup	XP_016857641.1:p.Gly336ArgfsTer?
XM_017002153.2:c.972dup	XP_016857642.1:p.Gly325ArgfsTer?
XM_024449295.1:c.891dup	XP_024305063.1:p.Gly298ArgfsTer?
NM_001024845.3:c.1086dup MANE Select	NP_001020016.1:p.Gly363ArgfsTer?
NM_001261380.2:c.1098dup	NP_001248309.1:p.Gly367ArgfsTer?
NM_001328626.2:c.753dup	NP_001315555.1:p.Gly252ArgfsTer?
NM_001328630.2:c.753dup	NP_001315559.1:p.Gly252ArgfsTer?
NM_006934.4:c.1143dup	NP_008865.2:p.Gly382ArgfsTer?
NM_201649.4:c.1305dup	NP_964012.2:p.Gly436ArgfsTer?
NR_048548.2:n.1173dup