Canonical Allele Identifier: CA2694793150

Gene: SLC9A6

Linked Data

• gnomAD v4: X-135985374-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985374T>C , CM000685.2:g.135985374T>C	GRCh38
NC_000023.10:g.135067533T>C , CM000685.1:g.135067533T>C	GRCh37
NC_000023.9:g.134895199T>C	NCBI36
NG_017160.1:g.4948T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-160T>C	ENSP00000359735.1:n.-160T>C
ENST00000636092.1:c.-56-229T>C	ENSP00000490406.1:n.-56-229T>C
ENST00000636347.1:c.-35-250T>C	ENSP00000490648.1:n.-35-250T>C
ENST00000637195.1:c.-35-250T>C	ENSP00000490330.1:n.-35-250T>C
ENST00000637234.1:c.-56-229T>C	ENSP00000490527.1:n.-56-229T>C
ENST00000637581.1:c.-56-229T>C	ENSP00000490731.1:n.-56-229T>C
XM_006724726.3:c.-155T>C	XP_006724789.1:n.-155T>C
XM_017029223.2:c.-56-229T>C	XP_016884712.1:n.-56-229T>C
XM_017029224.1:c.-56-229T>C	XP_016884713.1:n.-56-229T>C
NM_001400909.1:c.-35-250T>C	NP_001387838.1:n.-35-250T>C
NM_001400910.1:c.-56-229T>C	NP_001387839.1:n.-56-229T>C
NM_001400911.1:c.-56-229T>C	NP_001387840.1:n.-56-229T>C