Canonical Allele Identifier: CA1407538426

Gene: SLC9A9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143724269_143724274delinsCCCCTT , CM000665.2:g.143724269_143724274delinsCCCCTT	GRCh38
NC_000003.11:g.143443111_143443116delinsCCCCTT , CM000665.1:g.143443111_143443116delinsCCCCTT	GRCh37
NC_000003.10:g.144925801_144925806delinsCCCCTT	NCBI36
NG_017077.1:g.129258_129263delinsAAGGGG
NG_017077.2:g.129258_129263delinsAAGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.534-30967_534-30962delinsAAGGGG MANE Select	ENSP00000320246.6:n.534-30967_534-30962delinsAAGGGG
ENST00000316549.10:c.534-30967_534-30962delinsAAGGGG	ENSP00000320246.6:n.534-30967_534-30962delinsAAGGGG
ENST00000474727.2:c.*145-30967_*145-30962delinsAAGGGG	ENSP00000419090.2:n.*145-30967_*145-30962delinsAAGGGG
NM_173653.3:c.534-30967_534-30962delinsAAGGGG	NP_775924.1:n.534-30967_534-30962delinsAAGGGG
XM_011512704.1:c.534-30967_534-30962delinsAAGGGG	XP_011511006.1:n.534-30967_534-30962delinsAAGGGG
XM_011512704.3:c.534-30967_534-30962delinsAAGGGG	XP_011511006.1:n.534-30967_534-30962delinsAAGGGG
XM_017006202.2:c.534-30967_534-30962delinsAAGGGG	XP_016861691.1:n.534-30967_534-30962delinsAAGGGG
XM_017006203.1:c.183-30967_183-30962delinsAAGGGG	XP_016861692.1:n.183-30967_183-30962delinsAAGGGG
NM_173653.4:c.534-30967_534-30962delinsAAGGGG MANE Select	NP_775924.1:n.534-30967_534-30962delinsAAGGGG