Canonical Allele Identifier: CA1054439544

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1934011917
• gnomAD v3: 3-143707376-A-ACT
• gnomAD v4: 3-143707376-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707377_143707378insTC , CM000665.2:g.143707377_143707378insTC	GRCh38
NC_000003.11:g.143426219_143426220insTC , CM000665.1:g.143426219_143426220insTC	GRCh37
NC_000003.10:g.144908909_144908910insTC	NCBI36
NG_017077.1:g.146155_146156insAG
NG_017077.2:g.146155_146156insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14070_534-14069insAG MANE Select	ENSP00000320246.6:n.534-14070_534-14069insAG
ENST00000316549.10:c.534-14070_534-14069insAG	ENSP00000320246.6:n.534-14070_534-14069insAG
ENST00000474727.2:c.*145-14070_*145-14069insAG	ENSP00000419090.2:n.*145-14070_*145-14069insAG
NM_173653.3:c.534-14070_534-14069insAG	NP_775924.1:n.534-14070_534-14069insAG
XM_011512704.1:c.534-14070_534-14069insAG	XP_011511006.1:n.534-14070_534-14069insAG
XM_011512704.3:c.534-14070_534-14069insAG	XP_011511006.1:n.534-14070_534-14069insAG
XM_017006202.2:c.534-14070_534-14069insAG	XP_016861691.1:n.534-14070_534-14069insAG
XM_017006203.1:c.183-14070_183-14069insAG	XP_016861692.1:n.183-14070_183-14069insAG
NM_173653.4:c.534-14070_534-14069insAG MANE Select	NP_775924.1:n.534-14070_534-14069insAG