Canonical Allele Identifier: CA1407536505
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707060_143707061delinsTG , CM000665.2:g.143707060_143707061delinsTG GRCh38
NC_000003.11:g.143425902_143425903delinsTG , CM000665.1:g.143425902_143425903delinsTG GRCh37
NC_000003.10:g.144908592_144908593delinsTG NCBI36
NG_017077.1:g.146471_146472delinsCA
NG_017077.2:g.146471_146472delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-13754_534-13753delinsCA MANE Select ENSP00000320246.6:n.534-13754_534-13753delinsCA
ENST00000316549.10:c.534-13754_534-13753delinsCA ENSP00000320246.6:n.534-13754_534-13753delinsCA
ENST00000474727.2:c.*145-13754_*145-13753delinsCA ENSP00000419090.2:n.*145-13754_*145-13753delinsCA
NM_173653.3:c.534-13754_534-13753delinsCA NP_775924.1:n.534-13754_534-13753delinsCA
XM_011512704.1:c.534-13754_534-13753delinsCA XP_011511006.1:n.534-13754_534-13753delinsCA
XM_011512704.3:c.534-13754_534-13753delinsCA XP_011511006.1:n.534-13754_534-13753delinsCA
XM_017006202.2:c.534-13754_534-13753delinsCA XP_016861691.1:n.534-13754_534-13753delinsCA
XM_017006203.1:c.183-13754_183-13753delinsCA XP_016861692.1:n.183-13754_183-13753delinsCA
NM_173653.4:c.534-13754_534-13753delinsCA MANE Select NP_775924.1:n.534-13754_534-13753delinsCA