Canonical Allele Identifier: CA1054423697

Gene: SLC9A9

Linked Data

• gnomAD v3: 3-143724291-T-TACTAGAGCAATCACCCCTCACATATAACATCAAAGGTAGGATGCCAGGAGAGCCTTTCAGTG
• gnomAD v4: 3-143724291-T-TACTAGAGCAATCACCCCTCACATATAACATCAAAGGTAGGATGCCAGGAGAGCCTTTCAGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143724291_143724292insACTAGAGCAATCACCCCTCACATATAACATCAAAGGTAGGATGCCAGGAGAGCCTTTCAGTG , CM000665.2:g.143724291_143724292insACTAGAGCAATCACCCCTCACATATAACATCAAAGGTAGGATGCCAGGAGAGCCTTTCAGTG	GRCh38
NC_000003.11:g.143443133_143443134insACTAGAGCAATCACCCCTCACATATAACATCAAAGGTAGGATGCCAGGAGAGCCTTTCAGTG , CM000665.1:g.143443133_143443134insACTAGAGCAATCACCCCTCACATATAACATCAAAGGTAGGATGCCAGGAGAGCCTTTCAGTG	GRCh37
NC_000003.10:g.144925823_144925824insACTAGAGCAATCACCCCTCACATATAACATCAAAGGTAGGATGCCAGGAGAGCCTTTCAGTG	NCBI36
NG_017077.1:g.129240_129241insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT
NG_017077.2:g.129240_129241insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT MANE Select	ENSP00000320246.6:n.534-30985_534-30984insCACTGAAAGGCTCTCCTGG...
ENST00000316549.10:c.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT	ENSP00000320246.6:n.534-30985_534-30984insCACTGAAAGGCTCTCCTGG...
ENST00000474727.2:c.*145-30985_*145-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT	ENSP00000419090.2:n.*145-30985_*145-30984insCACTGAAAGGCTCTCCT...
NM_173653.3:c.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT	NP_775924.1:n.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCT...
XM_011512704.1:c.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT	XP_011511006.1:n.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCAT...
XM_011512704.3:c.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT	XP_011511006.1:n.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCAT...
XM_017006202.2:c.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT	XP_016861691.1:n.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCAT...
XM_017006203.1:c.183-30985_183-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT	XP_016861692.1:n.183-30985_183-30984insCACTGAAAGGCTCTCCTGGCAT...
NM_173653.4:c.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCTACCTTTGATGTTATATGTGAGGGGTGATTGCTCTAGT MANE Select	NP_775924.1:n.534-30985_534-30984insCACTGAAAGGCTCTCCTGGCATCCT...