Canonical Allele Identifier: CA1407536804

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707399_143707400delinsCA , CM000665.2:g.143707399_143707400delinsCA	GRCh38
NC_000003.11:g.143426241_143426242delinsCA , CM000665.1:g.143426241_143426242delinsCA	GRCh37
NC_000003.10:g.144908931_144908932delinsCA	NCBI36
NG_017077.1:g.146132_146133delinsTG
NG_017077.2:g.146132_146133delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14093_534-14092delinsTG MANE Select	ENSP00000320246.6:n.534-14093_534-14092delinsTG
ENST00000316549.10:c.534-14093_534-14092delinsTG	ENSP00000320246.6:n.534-14093_534-14092delinsTG
ENST00000474727.2:c.*145-14093_*145-14092delinsTG	ENSP00000419090.2:n.*145-14093_*145-14092delinsTG
NM_173653.3:c.534-14093_534-14092delinsTG	NP_775924.1:n.534-14093_534-14092delinsTG
XM_011512704.1:c.534-14093_534-14092delinsTG	XP_011511006.1:n.534-14093_534-14092delinsTG
XM_011512704.3:c.534-14093_534-14092delinsTG	XP_011511006.1:n.534-14093_534-14092delinsTG
XM_017006202.2:c.534-14093_534-14092delinsTG	XP_016861691.1:n.534-14093_534-14092delinsTG
XM_017006203.1:c.183-14093_183-14092delinsTG	XP_016861692.1:n.183-14093_183-14092delinsTG
NM_173653.4:c.534-14093_534-14092delinsTG MANE Select	NP_775924.1:n.534-14093_534-14092delinsTG