Canonical Allele Identifier: CA1054400497

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1938376960
• gnomAD v3: 3-143286192-C-T
• gnomAD v4: 3-143286192-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143286192C>T , CM000665.2:g.143286192C>T	GRCh38
NC_000003.11:g.143005034C>T , CM000665.1:g.143005034C>T	GRCh37
NC_000003.10:g.144487724C>T	NCBI36
NG_017077.1:g.567340G>A
NG_017077.2:g.567340G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1605-17212G>A MANE Select	ENSP00000320246.6:n.1605-17212G>A
ENST00000316549.10:c.1605-17212G>A	ENSP00000320246.6:n.1605-17212G>A
NM_173653.3:c.1605-17212G>A	NP_775924.1:n.1605-17212G>A
XM_011512703.1:c.957-17212G>A	XP_011511005.1:n.957-17212G>A
XM_011512703.3:c.957-17212G>A	XP_011511005.1:n.957-17212G>A
XM_017006202.2:c.1712-1850G>A	XP_016861691.1:n.1712-1850G>A
XM_017006203.1:c.1254-17212G>A	XP_016861692.1:n.1254-17212G>A
NM_173653.4:c.1605-17212G>A MANE Select	NP_775924.1:n.1605-17212G>A