Canonical Allele Identifier: CA1407536805

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707400_143707402delinsACC , CM000665.2:g.143707400_143707402delinsACC	GRCh38
NC_000003.11:g.143426242_143426244delinsACC , CM000665.1:g.143426242_143426244delinsACC	GRCh37
NC_000003.10:g.144908932_144908934delinsACC	NCBI36
NG_017077.1:g.146130_146132delinsGGT
NG_017077.2:g.146130_146132delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14095_534-14093delinsGGT MANE Select	ENSP00000320246.6:n.534-14095_534-14093delinsGGT
ENST00000316549.10:c.534-14095_534-14093delinsGGT	ENSP00000320246.6:n.534-14095_534-14093delinsGGT
ENST00000474727.2:c.*145-14095_*145-14093delinsGGT	ENSP00000419090.2:n.*145-14095_*145-14093delinsGGT
NM_173653.3:c.534-14095_534-14093delinsGGT	NP_775924.1:n.534-14095_534-14093delinsGGT
XM_011512704.1:c.534-14095_534-14093delinsGGT	XP_011511006.1:n.534-14095_534-14093delinsGGT
XM_011512704.3:c.534-14095_534-14093delinsGGT	XP_011511006.1:n.534-14095_534-14093delinsGGT
XM_017006202.2:c.534-14095_534-14093delinsGGT	XP_016861691.1:n.534-14095_534-14093delinsGGT
XM_017006203.1:c.183-14095_183-14093delinsGGT	XP_016861692.1:n.183-14095_183-14093delinsGGT
NM_173653.4:c.534-14095_534-14093delinsGGT MANE Select	NP_775924.1:n.534-14095_534-14093delinsGGT