Canonical Allele Identifier: CA2694793106

Gene: SLC9A6

Linked Data

• gnomAD v4: X-135985332-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985332A>C , CM000685.2:g.135985332A>C	GRCh38
NC_000023.10:g.135067491A>C , CM000685.1:g.135067491A>C	GRCh37
NC_000023.9:g.134895157A>C	NCBI36
NG_017160.1:g.4906A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-202A>C	ENSP00000359735.1:n.-202A>C
ENST00000636092.1:c.-56-271A>C	ENSP00000490406.1:n.-56-271A>C
ENST00000636347.1:c.-35-292A>C	ENSP00000490648.1:n.-35-292A>C
ENST00000637195.1:c.-35-292A>C	ENSP00000490330.1:n.-35-292A>C
ENST00000637234.1:c.-56-271A>C	ENSP00000490527.1:n.-56-271A>C
ENST00000637581.1:c.-56-271A>C	ENSP00000490731.1:n.-56-271A>C
XM_006724726.3:c.-197A>C	XP_006724789.1:n.-197A>C
XM_017029223.2:c.-56-271A>C	XP_016884712.1:n.-56-271A>C
XM_017029224.1:c.-56-271A>C	XP_016884713.1:n.-56-271A>C
NM_001400909.1:c.-35-292A>C	NP_001387838.1:n.-35-292A>C
NM_001400910.1:c.-56-271A>C	NP_001387839.1:n.-56-271A>C
NM_001400911.1:c.-56-271A>C	NP_001387840.1:n.-56-271A>C