Canonical Allele Identifier: CA2605098565

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2108793593
• gnomAD v3: 3-143707214-C-CT
• gnomAD v4: 3-143707214-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707216dup , CM000665.2:g.143707216dup	GRCh38
NC_000003.11:g.143426058dup , CM000665.1:g.143426058dup	GRCh37
NC_000003.10:g.144908748dup	NCBI36
NG_017077.1:g.146317dup
NG_017077.2:g.146317dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-13908dup MANE Select	ENSP00000320246.6:n.534-13908dup
ENST00000316549.10:c.534-13908dup	ENSP00000320246.6:n.534-13908dup
ENST00000474727.2:c.*145-13908dup	ENSP00000419090.2:n.*145-13908dup
NM_173653.3:c.534-13908dup	NP_775924.1:n.534-13908dup
XM_011512704.1:c.534-13908dup	XP_011511006.1:n.534-13908dup
XM_011512704.3:c.534-13908dup	XP_011511006.1:n.534-13908dup
XM_017006202.2:c.534-13908dup	XP_016861691.1:n.534-13908dup
XM_017006203.1:c.183-13908dup	XP_016861692.1:n.183-13908dup
NM_173653.4:c.534-13908dup MANE Select	NP_775924.1:n.534-13908dup