Canonical Allele Identifier: CA546822627
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1168921117

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707127G>A , CM000665.2:g.143707127G>A GRCh38
NC_000003.11:g.143425969G>A , CM000665.1:g.143425969G>A GRCh37
NC_000003.10:g.144908659G>A NCBI36
NG_017077.1:g.146405C>T
NG_017077.2:g.146405C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-13820C>T MANE Select ENSP00000320246.6:n.534-13820C>T
ENST00000316549.10:c.534-13820C>T ENSP00000320246.6:n.534-13820C>T
ENST00000474727.2:c.*145-13820C>T ENSP00000419090.2:n.*145-13820C>T
NM_173653.3:c.534-13820C>T NP_775924.1:n.534-13820C>T
XM_011512704.1:c.534-13820C>T XP_011511006.1:n.534-13820C>T
XM_011512704.3:c.534-13820C>T XP_011511006.1:n.534-13820C>T
XM_017006202.2:c.534-13820C>T XP_016861691.1:n.534-13820C>T
XM_017006203.1:c.183-13820C>T XP_016861692.1:n.183-13820C>T
NM_173653.4:c.534-13820C>T MANE Select NP_775924.1:n.534-13820C>T