Canonical Allele Identifier: CA2758721007
Gene: SLC9A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143302150G>C , CM000665.2:g.143302150G>C GRCh38
NC_000003.11:g.143020992G>C , CM000665.1:g.143020992G>C GRCh37
NC_000003.10:g.144503682G>C NCBI36
NG_017077.1:g.551382C>G
NG_017077.2:g.551382C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1605-33170C>G MANE Select ENSP00000320246.6:n.1605-33170C>G
ENST00000316549.10:c.1605-33170C>G ENSP00000320246.6:n.1605-33170C>G
NM_173653.3:c.1605-33170C>G NP_775924.1:n.1605-33170C>G
XM_011512703.1:c.957-33170C>G XP_011511005.1:n.957-33170C>G
XM_011512703.3:c.957-33170C>G XP_011511005.1:n.957-33170C>G
XM_017006202.2:c.1712-17808C>G XP_016861691.1:n.1712-17808C>G
XM_017006203.1:c.1254-33170C>G XP_016861692.1:n.1254-33170C>G
NM_173653.4:c.1605-33170C>G MANE Select NP_775924.1:n.1605-33170C>G