Canonical Allele Identifier: CA2758721006
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143302110C>A , CM000665.2:g.143302110C>A GRCh38
NC_000003.11:g.143020952C>A , CM000665.1:g.143020952C>A GRCh37
NC_000003.10:g.144503642C>A NCBI36
NG_017077.1:g.551422G>T
NG_017077.2:g.551422G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1605-33130G>T MANE Select ENSP00000320246.6:n.1605-33130G>T
ENST00000316549.10:c.1605-33130G>T ENSP00000320246.6:n.1605-33130G>T
NM_173653.3:c.1605-33130G>T NP_775924.1:n.1605-33130G>T
XM_011512703.1:c.957-33130G>T XP_011511005.1:n.957-33130G>T
XM_011512703.3:c.957-33130G>T XP_011511005.1:n.957-33130G>T
XM_017006202.2:c.1712-17768G>T XP_016861691.1:n.1712-17768G>T
XM_017006203.1:c.1254-33130G>T XP_016861692.1:n.1254-33130G>T
NM_173653.4:c.1605-33130G>T MANE Select NP_775924.1:n.1605-33130G>T