Canonical Allele Identifier: CA1407372350

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337564_143337565delinsAC , CM000665.2:g.143337564_143337565delinsAC	GRCh38
NC_000003.11:g.143056406_143056407delinsAC , CM000665.1:g.143056406_143056407delinsAC	GRCh37
NC_000003.10:g.144539096_144539097delinsAC	NCBI36
NG_017077.1:g.515967_515968delinsGT
NG_017077.2:g.515967_515968delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+25919_1604+25920delinsGT MANE Select	ENSP00000320246.6:n.1604+25919_1604+25920delinsGT
ENST00000316549.10:c.1604+25919_1604+25920delinsGT	ENSP00000320246.6:n.1604+25919_1604+25920delinsGT
NM_173653.3:c.1604+25919_1604+25920delinsGT	NP_775924.1:n.1604+25919_1604+25920delinsGT
XM_011512703.1:c.956+25919_956+25920delinsGT	XP_011511005.1:n.956+25919_956+25920delinsGT
XM_011512703.3:c.956+25919_956+25920delinsGT	XP_011511005.1:n.956+25919_956+25920delinsGT
XM_017006202.2:c.1711+25812_1711+25813delinsGT	XP_016861691.1:n.1711+25812_1711+25813delinsGT
XM_017006203.1:c.1253+25919_1253+25920delinsGT	XP_016861692.1:n.1253+25919_1253+25920delinsGT
NM_173653.4:c.1604+25919_1604+25920delinsGT MANE Select	NP_775924.1:n.1604+25919_1604+25920delinsGT