Canonical Allele Identifier: CA1054400498
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1938377166
gnomAD v3: 3-143286215-T-TC
gnomAD v4: 3-143286215-T-TC
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286215_143286216insC , CM000665.2:g.143286215_143286216insC GRCh38
NC_000003.11:g.143005057_143005058insC , CM000665.1:g.143005057_143005058insC GRCh37
NC_000003.10:g.144487747_144487748insC NCBI36
NG_017077.1:g.567316_567317insG
NG_017077.2:g.567316_567317insG

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-17236_1605-17235insG MANE Select ENSP00000320246.6:n.1605-17236_1605-17235...
ENST00000316549.10:c.1605-17236_1605-17235insG ENSP00000320246.6:n.1605-17236_1605-17235...
NM_173653.3:c.1605-17236_1605-17235insG NP_775924.1:n.1605-17236_1605-17235insG
XM_011512703.1:c.957-17236_957-17235insG XP_011511005.1:n.957-17236_957-17235insG
XM_011512703.3:c.957-17236_957-17235insG XP_011511005.1:n.957-17236_957-17235insG
XM_017006202.2:c.1712-1874_1712-1873insG XP_016861691.1:n.1712-1874_1712-1873insG
XM_017006203.1:c.1254-17236_1254-17235insG XP_016861692.1:n.1254-17236_1254-17235ins...
NM_173653.4:c.1605-17236_1605-17235insG MANE Select NP_775924.1:n.1605-17236_1605-17235insG
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