Canonical Allele Identifier: CA2758721752

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337595_143337596insTTT , CM000665.2:g.143337595_143337596insTTT	GRCh38
NC_000003.11:g.143056437_143056438insTTT , CM000665.1:g.143056437_143056438insTTT	GRCh37
NC_000003.10:g.144539127_144539128insTTT	NCBI36
NG_017077.1:g.515936_515937insAAA
NG_017077.2:g.515936_515937insAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1604+25888_1604+25889insAAA MANE Select	ENSP00000320246.6:n.1604+25888_1604+25889insAAA
ENST00000316549.10:c.1604+25888_1604+25889insAAA	ENSP00000320246.6:n.1604+25888_1604+25889insAAA
NM_173653.3:c.1604+25888_1604+25889insAAA	NP_775924.1:n.1604+25888_1604+25889insAAA
XM_011512703.1:c.956+25888_956+25889insAAA	XP_011511005.1:n.956+25888_956+25889insAAA
XM_011512703.3:c.956+25888_956+25889insAAA	XP_011511005.1:n.956+25888_956+25889insAAA
XM_017006202.2:c.1711+25781_1711+25782insAAA	XP_016861691.1:n.1711+25781_1711+25782insAAA
XM_017006203.1:c.1253+25888_1253+25889insAAA	XP_016861692.1:n.1253+25888_1253+25889insAAA
NM_173653.4:c.1604+25888_1604+25889insAAA MANE Select	NP_775924.1:n.1604+25888_1604+25889insAAA