Canonical Allele Identifier: CA2758721757

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337617_143337618insA , CM000665.2:g.143337617_143337618insA	GRCh38
NC_000003.11:g.143056459_143056460insA , CM000665.1:g.143056459_143056460insA	GRCh37
NC_000003.10:g.144539149_144539150insA	NCBI36
NG_017077.1:g.515914_515915insT
NG_017077.2:g.515914_515915insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+25866_1604+25867insT MANE Select	ENSP00000320246.6:n.1604+25866_1604+25867insT
ENST00000316549.10:c.1604+25866_1604+25867insT	ENSP00000320246.6:n.1604+25866_1604+25867insT
NM_173653.3:c.1604+25866_1604+25867insT	NP_775924.1:n.1604+25866_1604+25867insT
XM_011512703.1:c.956+25866_956+25867insT	XP_011511005.1:n.956+25866_956+25867insT
XM_011512703.3:c.956+25866_956+25867insT	XP_011511005.1:n.956+25866_956+25867insT
XM_017006202.2:c.1711+25759_1711+25760insT	XP_016861691.1:n.1711+25759_1711+25760insT
XM_017006203.1:c.1253+25866_1253+25867insT	XP_016861692.1:n.1253+25866_1253+25867insT
NM_173653.4:c.1604+25866_1604+25867insT MANE Select	NP_775924.1:n.1604+25866_1604+25867insT