Canonical Allele Identifier: CA1407571660
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1156734058

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143785742G>C , CM000665.2:g.143785742G>C GRCh38
NC_000003.11:g.143504584G>C , CM000665.1:g.143504584G>C GRCh37
NC_000003.10:g.144987274G>C NCBI36
NG_017077.1:g.67790C>G
NG_017077.2:g.67790C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.533+9259C>G MANE Select ENSP00000320246.6:n.533+9259C>G
ENST00000316549.10:c.533+9259C>G ENSP00000320246.6:n.533+9259C>G
ENST00000474727.2:c.*144+9259C>G ENSP00000419090.2:n.*144+9259C>G
NM_173653.3:c.533+9259C>G NP_775924.1:n.533+9259C>G
XM_011512704.1:c.533+9259C>G XP_011511006.1:n.533+9259C>G
XM_011512704.3:c.533+9259C>G XP_011511006.1:n.533+9259C>G
XM_017006202.2:c.533+9259C>G XP_016861691.1:n.533+9259C>G
XM_017006203.1:c.182+9259C>G XP_016861692.1:n.182+9259C>G
NM_173653.4:c.533+9259C>G MANE Select NP_775924.1:n.533+9259C>G