Canonical Allele Identifier: CA11381109

Gene: SLC9A9

Linked Data

• dbSNP Id: rs9815453
• gnomAD v2: 3-143443105-C-G
• gnomAD v3: 3-143724263-C-G
• gnomAD v4: 3-143724263-C-G
• MyVariant Identifiers: chr3:g.143443105C>G (hg19) ; chr3:g.143724263C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143724263C>G , CM000665.2:g.143724263C>G	GRCh38
NC_000003.11:g.143443105C>G , CM000665.1:g.143443105C>G	GRCh37
NC_000003.10:g.144925795C>G	NCBI36
NG_017077.1:g.129269G>C
NG_017077.2:g.129269G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.534-30956G>C MANE Select	ENSP00000320246.6:n.534-30956G>C
ENST00000316549.10:c.534-30956G>C	ENSP00000320246.6:n.534-30956G>C
ENST00000474727.2:c.*145-30956G>C	ENSP00000419090.2:n.*145-30956G>C
NM_173653.3:c.534-30956G>C	NP_775924.1:n.534-30956G>C
XM_011512704.1:c.534-30956G>C	XP_011511006.1:n.534-30956G>C
XM_011512704.3:c.534-30956G>C	XP_011511006.1:n.534-30956G>C
XM_017006202.2:c.534-30956G>C	XP_016861691.1:n.534-30956G>C
XM_017006203.1:c.183-30956G>C	XP_016861692.1:n.183-30956G>C
NM_173653.4:c.534-30956G>C MANE Select	NP_775924.1:n.534-30956G>C