Canonical Allele Identifier: CA1407571684
Gene: SLC9A9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143785793G= , CM000665.2:g.143785793G= GRCh38
NC_000003.11:g.143504635G= , CM000665.1:g.143504635G= GRCh37
NC_000003.10:g.144987325G= NCBI36
NG_017077.1:g.67739C=
NG_017077.2:g.67739C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.533+9208C= MANE Select ENSP00000320246.6:n.533+9208C=
ENST00000316549.10:c.533+9208C= ENSP00000320246.6:n.533+9208C=
ENST00000474727.2:c.*144+9208C= ENSP00000419090.2:n.*144+9208C=
NM_173653.3:c.533+9208C= NP_775924.1:n.533+9208C=
XM_011512704.1:c.533+9208C= XP_011511006.1:n.533+9208C=
XM_011512704.3:c.533+9208C= XP_011511006.1:n.533+9208C=
XM_017006202.2:c.533+9208C= XP_016861691.1:n.533+9208C=
XM_017006203.1:c.182+9208C= XP_016861692.1:n.182+9208C=
NM_173653.4:c.533+9208C= MANE Select NP_775924.1:n.533+9208C=
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