Canonical Allele Identifier: CA1407535400
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1933957855

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705908_143705912dup , CM000665.2:g.143705908_143705912dup GRCh38
NC_000003.11:g.143424750_143424754dup , CM000665.1:g.143424750_143424754dup GRCh37
NC_000003.10:g.144907440_144907444dup NCBI36
NG_017077.1:g.147622_147626dup
NG_017077.2:g.147622_147626dup

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.534-12603_534-12599dup MANE Select ENSP00000320246.6:n.534-12603_534-12599du...
ENST00000316549.10:c.534-12603_534-12599dup ENSP00000320246.6:n.534-12603_534-12599du...
ENST00000474727.2:c.*145-12603_*145-12599dup ENSP00000419090.2:n.*145-12603_*145-12599...
NM_173653.3:c.534-12603_534-12599dup NP_775924.1:n.534-12603_534-12599dup
XM_011512704.1:c.534-12603_534-12599dup XP_011511006.1:n.534-12603_534-12599dup
XM_011512704.3:c.534-12603_534-12599dup XP_011511006.1:n.534-12603_534-12599dup
XM_017006202.2:c.534-12603_534-12599dup XP_016861691.1:n.534-12603_534-12599dup
XM_017006203.1:c.183-12603_183-12599dup XP_016861692.1:n.183-12603_183-12599dup
NM_173653.4:c.534-12603_534-12599dup MANE Select NP_775924.1:n.534-12603_534-12599dup