Canonical Allele Identifier: CA2694793175

Gene: SLC9A6

Linked Data

• gnomAD v4: X-135985391-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985391G>A , CM000685.2:g.135985391G>A	GRCh38
NC_000023.10:g.135067550G>A , CM000685.1:g.135067550G>A	GRCh37
NC_000023.9:g.134895216G>A	NCBI36
NG_017160.1:g.4965G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-143G>A	ENSP00000359735.1:n.-143G>A
ENST00000636092.1:c.-56-212G>A	ENSP00000490406.1:n.-56-212G>A
ENST00000636347.1:c.-35-233G>A	ENSP00000490648.1:n.-35-233G>A
ENST00000637195.1:c.-35-233G>A	ENSP00000490330.1:n.-35-233G>A
ENST00000637234.1:c.-56-212G>A	ENSP00000490527.1:n.-56-212G>A
ENST00000637581.1:c.-56-212G>A	ENSP00000490731.1:n.-56-212G>A
XM_006724726.3:c.-138G>A	XP_006724789.1:n.-138G>A
XM_017029223.2:c.-56-212G>A	XP_016884712.1:n.-56-212G>A
XM_017029224.1:c.-56-212G>A	XP_016884713.1:n.-56-212G>A
NM_001400909.1:c.-35-233G>A	NP_001387838.1:n.-35-233G>A
NM_001400910.1:c.-56-212G>A	NP_001387839.1:n.-56-212G>A
NM_001400911.1:c.-56-212G>A	NP_001387840.1:n.-56-212G>A