Canonical Allele Identifier: CA2579709443

Gene: SLC9A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985433G>A , CM000685.2:g.135985433G>A	GRCh38
NC_000023.10:g.135067592G>A , CM000685.1:g.135067592G>A	GRCh37
NC_000023.9:g.134895258G>A	NCBI36
NG_017160.1:g.5007G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-101G>A	ENSP00000359735.1:n.-101G>A
ENST00000636092.1:c.-56-170G>A	ENSP00000490406.1:n.-56-170G>A
ENST00000636347.1:c.-35-191G>A	ENSP00000490648.1:n.-35-191G>A
ENST00000637195.1:c.-35-191G>A	ENSP00000490330.1:n.-35-191G>A
ENST00000637234.1:c.-56-170G>A	ENSP00000490527.1:n.-56-170G>A
ENST00000637581.1:c.-56-170G>A	ENSP00000490731.1:n.-56-170G>A
ENST00000370698.7:c.-70G>A	ENSP00000359732.3:n.-70G>A
ENST00000370701.5:c.-101G>A	ENSP00000359735.1:n.-101G>A
ENST00000627534.2:c.-96G>A	ENSP00000486743.1:n.-96G>A
NM_001042537.1:c.-70G>A	NP_001036002.1:n.-70G>A
NM_001177651.1:c.-101G>A	NP_001171122.1:n.-101G>A
NM_006359.2:c.-70G>A	NP_006350.1:n.-70G>A
NM_001330652.1:c.-96G>A	NP_001317581.1:n.-96G>A
XM_006724726.3:c.-96G>A	XP_006724789.1:n.-96G>A
XM_017029223.2:c.-56-170G>A	XP_016884712.1:n.-56-170G>A
XM_017029224.1:c.-56-170G>A	XP_016884713.1:n.-56-170G>A
XM_017029225.1:c.-101G>A	XP_016884714.1:n.-101G>A
NM_001400909.1:c.-35-191G>A	NP_001387838.1:n.-35-191G>A
NM_001400910.1:c.-56-170G>A	NP_001387839.1:n.-56-170G>A
NM_001400911.1:c.-56-170G>A	NP_001387840.1:n.-56-170G>A