Canonical Allele Identifier: CA2579709444

Gene: SLC9A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985434T>G , CM000685.2:g.135985434T>G	GRCh38
NC_000023.10:g.135067593T>G , CM000685.1:g.135067593T>G	GRCh37
NC_000023.9:g.134895259T>G	NCBI36
NG_017160.1:g.5008T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-100T>G	ENSP00000359735.1:n.-100T>G
ENST00000636092.1:c.-56-169T>G	ENSP00000490406.1:n.-56-169T>G
ENST00000636347.1:c.-35-190T>G	ENSP00000490648.1:n.-35-190T>G
ENST00000637195.1:c.-35-190T>G	ENSP00000490330.1:n.-35-190T>G
ENST00000637234.1:c.-56-169T>G	ENSP00000490527.1:n.-56-169T>G
ENST00000637581.1:c.-56-169T>G	ENSP00000490731.1:n.-56-169T>G
ENST00000370698.7:c.-69T>G	ENSP00000359732.3:n.-69T>G
ENST00000370701.5:c.-100T>G	ENSP00000359735.1:n.-100T>G
ENST00000627534.2:c.-95T>G	ENSP00000486743.1:n.-95T>G
NM_001042537.1:c.-69T>G	NP_001036002.1:n.-69T>G
NM_001177651.1:c.-100T>G	NP_001171122.1:n.-100T>G
NM_006359.2:c.-69T>G	NP_006350.1:n.-69T>G
NM_001330652.1:c.-95T>G	NP_001317581.1:n.-95T>G
XM_006724726.3:c.-95T>G	XP_006724789.1:n.-95T>G
XM_017029223.2:c.-56-169T>G	XP_016884712.1:n.-56-169T>G
XM_017029224.1:c.-56-169T>G	XP_016884713.1:n.-56-169T>G
XM_017029225.1:c.-100T>G	XP_016884714.1:n.-100T>G
NM_001400909.1:c.-35-190T>G	NP_001387838.1:n.-35-190T>G
NM_001400910.1:c.-56-169T>G	NP_001387839.1:n.-56-169T>G
NM_001400911.1:c.-56-169T>G	NP_001387840.1:n.-56-169T>G