Canonical Allele Identifier: CA1407535390

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143705892_143705897delinsTTTTCC , CM000665.2:g.143705892_143705897delinsTTTTCC	GRCh38
NC_000003.11:g.143424734_143424739delinsTTTTCC , CM000665.1:g.143424734_143424739delinsTTTTCC	GRCh37
NC_000003.10:g.144907424_144907429delinsTTTTCC	NCBI36
NG_017077.1:g.147635_147640delinsGGAAAA
NG_017077.2:g.147635_147640delinsGGAAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.534-12590_534-12585delinsGGAAAA MANE Select	ENSP00000320246.6:n.534-12590_534-12585de...
ENST00000316549.10:c.534-12590_534-12585delinsGGAAAA	ENSP00000320246.6:n.534-12590_534-12585de...
ENST00000474727.2:c.*145-12590_*145-12585delinsGGAAAA	ENSP00000419090.2:n.*145-12590_*145-12585...
NM_173653.3:c.534-12590_534-12585delinsGGAAAA	NP_775924.1:n.534-12590_534-12585delinsGG...
XM_011512704.1:c.534-12590_534-12585delinsGGAAAA	XP_011511006.1:n.534-12590_534-12585delin...
XM_011512704.3:c.534-12590_534-12585delinsGGAAAA	XP_011511006.1:n.534-12590_534-12585delin...
XM_017006202.2:c.534-12590_534-12585delinsGGAAAA	XP_016861691.1:n.534-12590_534-12585delin...
XM_017006203.1:c.183-12590_183-12585delinsGGAAAA	XP_016861692.1:n.183-12590_183-12585delin...
NM_173653.4:c.534-12590_534-12585delinsGGAAAA MANE Select	NP_775924.1:n.534-12590_534-12585delinsGG...