Canonical Allele Identifier: CA1054402461
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs2030546494

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143302064dup , CM000665.2:g.143302064dup GRCh38
NC_000003.11:g.143020906dup , CM000665.1:g.143020906dup GRCh37
NC_000003.10:g.144503596dup NCBI36
NG_017077.1:g.551468dup
NG_017077.2:g.551468dup

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-33084dup MANE Select ENSP00000320246.6:n.1605-33084dup
ENST00000316549.10:c.1605-33084dup ENSP00000320246.6:n.1605-33084dup
NM_173653.3:c.1605-33084dup NP_775924.1:n.1605-33084dup
XM_011512703.1:c.957-33084dup XP_011511005.1:n.957-33084dup
XM_011512703.3:c.957-33084dup XP_011511005.1:n.957-33084dup
XM_017006202.2:c.1712-17722dup XP_016861691.1:n.1712-17722dup
XM_017006203.1:c.1254-33084dup XP_016861692.1:n.1254-33084dup
NM_173653.4:c.1605-33084dup MANE Select NP_775924.1:n.1605-33084dup