Canonical Allele Identifier: CA2460185288

Gene: SLC9A6

Linked Data

• dbSNP Id: rs2089313738

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985388_135985397del , CM000685.2:g.135985388_135985397del	GRCh38
NC_000023.10:g.135067547_135067556del , CM000685.1:g.135067547_135067556del	GRCh37
NC_000023.9:g.134895213_134895222del	NCBI36
NG_017160.1:g.4962_4971del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-146_-137del	ENSP00000359735.1:n.-146_-137del
ENST00000636092.1:c.-56-215_-56-206del	ENSP00000490406.1:n.-56-215_-56-206del
ENST00000636347.1:c.-35-236_-35-227del	ENSP00000490648.1:n.-35-236_-35-227del
ENST00000637195.1:c.-35-236_-35-227del	ENSP00000490330.1:n.-35-236_-35-227del
ENST00000637234.1:c.-56-215_-56-206del	ENSP00000490527.1:n.-56-215_-56-206del
ENST00000637581.1:c.-56-215_-56-206del	ENSP00000490731.1:n.-56-215_-56-206del
XM_006724726.3:c.-141_-132del	XP_006724789.1:n.-141_-132del
XM_017029223.2:c.-56-215_-56-206del	XP_016884712.1:n.-56-215_-56-206del
XM_017029224.1:c.-56-215_-56-206del	XP_016884713.1:n.-56-215_-56-206del
NM_001400909.1:c.-35-236_-35-227del	NP_001387838.1:n.-35-236_-35-227del
NM_001400910.1:c.-56-215_-56-206del	NP_001387839.1:n.-56-215_-56-206del
NM_001400911.1:c.-56-215_-56-206del	NP_001387840.1:n.-56-215_-56-206del