Canonical Allele Identifier: CA917025857

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1553782892

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707391_143707392insCA , CM000665.2:g.143707391_143707392insCA	GRCh38
NC_000003.11:g.143426233_143426234insCA , CM000665.1:g.143426233_143426234insCA	GRCh37
NC_000003.10:g.144908923_144908924insCA	NCBI36
NG_017077.1:g.146140_146141insTG
NG_017077.2:g.146140_146141insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14085_534-14084insTG MANE Select	ENSP00000320246.6:n.534-14085_534-14084insTG
ENST00000316549.10:c.534-14085_534-14084insTG	ENSP00000320246.6:n.534-14085_534-14084insTG
ENST00000474727.2:c.*145-14085_*145-14084insTG	ENSP00000419090.2:n.*145-14085_*145-14084insTG
NM_173653.3:c.534-14085_534-14084insTG	NP_775924.1:n.534-14085_534-14084insTG
XM_011512704.1:c.534-14085_534-14084insTG	XP_011511006.1:n.534-14085_534-14084insTG
XM_011512704.3:c.534-14085_534-14084insTG	XP_011511006.1:n.534-14085_534-14084insTG
XM_017006202.2:c.534-14085_534-14084insTG	XP_016861691.1:n.534-14085_534-14084insTG
XM_017006203.1:c.183-14085_183-14084insTG	XP_016861692.1:n.183-14085_183-14084insTG
NM_173653.4:c.534-14085_534-14084insTG MANE Select	NP_775924.1:n.534-14085_534-14084insTG