Canonical Allele Identifier: CA1407536854

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707439_143707443delinsCAAGT , CM000665.2:g.143707439_143707443delinsCAAGT	GRCh38
NC_000003.11:g.143426281_143426285delinsCAAGT , CM000665.1:g.143426281_143426285delinsCAAGT	GRCh37
NC_000003.10:g.144908971_144908975delinsCAAGT	NCBI36
NG_017077.1:g.146089_146093delinsACTTG
NG_017077.2:g.146089_146093delinsACTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-14136_534-14132delinsACTTG MANE Select	ENSP00000320246.6:n.534-14136_534-14132delinsACTTG
ENST00000316549.10:c.534-14136_534-14132delinsACTTG	ENSP00000320246.6:n.534-14136_534-14132delinsACTTG
ENST00000474727.2:c.*145-14136_*145-14132delinsACTTG	ENSP00000419090.2:n.*145-14136_*145-14132delinsACTTG
NM_173653.3:c.534-14136_534-14132delinsACTTG	NP_775924.1:n.534-14136_534-14132delinsACTTG
XM_011512704.1:c.534-14136_534-14132delinsACTTG	XP_011511006.1:n.534-14136_534-14132delinsACTTG
XM_011512704.3:c.534-14136_534-14132delinsACTTG	XP_011511006.1:n.534-14136_534-14132delinsACTTG
XM_017006202.2:c.534-14136_534-14132delinsACTTG	XP_016861691.1:n.534-14136_534-14132delinsACTTG
XM_017006203.1:c.183-14136_183-14132delinsACTTG	XP_016861692.1:n.183-14136_183-14132delinsACTTG
NM_173653.4:c.534-14136_534-14132delinsACTTG MANE Select	NP_775924.1:n.534-14136_534-14132delinsACTTG