Canonical Allele Identifier: CA1054402431

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2030541534
• gnomAD v3: 3-143301950-T-A
• gnomAD v4: 3-143301950-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143301950T>A , CM000665.2:g.143301950T>A	GRCh38
NC_000003.11:g.143020792T>A , CM000665.1:g.143020792T>A	GRCh37
NC_000003.10:g.144503482T>A	NCBI36
NG_017077.1:g.551582A>T
NG_017077.2:g.551582A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1605-32970A>T MANE Select	ENSP00000320246.6:n.1605-32970A>T
ENST00000316549.10:c.1605-32970A>T	ENSP00000320246.6:n.1605-32970A>T
NM_173653.3:c.1605-32970A>T	NP_775924.1:n.1605-32970A>T
XM_011512703.1:c.957-32970A>T	XP_011511005.1:n.957-32970A>T
XM_011512703.3:c.957-32970A>T	XP_011511005.1:n.957-32970A>T
XM_017006202.2:c.1712-17608A>T	XP_016861691.1:n.1712-17608A>T
XM_017006203.1:c.1254-32970A>T	XP_016861692.1:n.1254-32970A>T
NM_173653.4:c.1605-32970A>T MANE Select	NP_775924.1:n.1605-32970A>T