Canonical Allele Identifier: CA1054438760
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1933956274

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705867A>G , CM000665.2:g.143705867A>G GRCh38
NC_000003.11:g.143424709A>G , CM000665.1:g.143424709A>G GRCh37
NC_000003.10:g.144907399A>G NCBI36
NG_017077.1:g.147665T>C
NG_017077.2:g.147665T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-12560T>C MANE Select ENSP00000320246.6:n.534-12560T>C
ENST00000316549.10:c.534-12560T>C ENSP00000320246.6:n.534-12560T>C
ENST00000474727.2:c.*145-12560T>C ENSP00000419090.2:n.*145-12560T>C
NM_173653.3:c.534-12560T>C NP_775924.1:n.534-12560T>C
XM_011512704.1:c.534-12560T>C XP_011511006.1:n.534-12560T>C
XM_011512704.3:c.534-12560T>C XP_011511006.1:n.534-12560T>C
XM_017006202.2:c.534-12560T>C XP_016861691.1:n.534-12560T>C
XM_017006203.1:c.183-12560T>C XP_016861692.1:n.183-12560T>C
NM_173653.4:c.534-12560T>C MANE Select NP_775924.1:n.534-12560T>C