Canonical Allele Identifier: CA900032097

Gene: SLC9A9

Linked Data

• dbSNP Id: rs549058822
• gnomAD v3: 3-143707400-A-ACACACCCC
• gnomAD v4: 3-143707400-A-ACACACCCC
• MyVariant Identifiers: chr3:g.143426242_143426243insCACACCCC (hg19) ; chr3:g.143707400_143707401insCACACCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707401_143707402insACACCCCC , CM000665.2:g.143707401_143707402insACACCCCC	GRCh38
NC_000003.11:g.143426243_143426244insACACCCCC , CM000665.1:g.143426243_143426244insACACCCCC	GRCh37
NC_000003.10:g.144908933_144908934insACACCCCC	NCBI36
NG_017077.1:g.146131_146132insGGGGTGTG
NG_017077.2:g.146131_146132insGGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14094_534-14093insGGGGTGTG MANE Select	ENSP00000320246.6:n.534-14094_534-14093insGGGGTGTG
ENST00000316549.10:c.534-14094_534-14093insGGGGTGTG	ENSP00000320246.6:n.534-14094_534-14093insGGGGTGTG
ENST00000474727.2:c.*145-14094_*145-14093insGGGGTGTG	ENSP00000419090.2:n.*145-14094_*145-14093insGGGGTGTG
NM_173653.3:c.534-14094_534-14093insGGGGTGTG	NP_775924.1:n.534-14094_534-14093insGGGGTGTG
XM_011512704.1:c.534-14094_534-14093insGGGGTGTG	XP_011511006.1:n.534-14094_534-14093insGGGGTGTG
XM_011512704.3:c.534-14094_534-14093insGGGGTGTG	XP_011511006.1:n.534-14094_534-14093insGGGGTGTG
XM_017006202.2:c.534-14094_534-14093insGGGGTGTG	XP_016861691.1:n.534-14094_534-14093insGGGGTGTG
XM_017006203.1:c.183-14094_183-14093insGGGGTGTG	XP_016861692.1:n.183-14094_183-14093insGGGGTGTG
NM_173653.4:c.534-14094_534-14093insGGGGTGTG MANE Select	NP_775924.1:n.534-14094_534-14093insGGGGTGTG