Canonical Allele Identifier: CA85301872
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs60762977
gnomAD v2: 3-143426242-A-ACC
gnomAD v3: 3-143707400-A-ACC
gnomAD v4: 3-143707400-A-ACC
MyVariant Identifiers: chr3:g.143426243_143426244insCC (hg19) chr3:g.143426242_143426243insCC (hg19) chr3:g.143707401_143707402insCC (hg38) chr3:g.143707400_143707401insCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707403_143707404dup , CM000665.2:g.143707403_143707404dup GRCh38
NC_000003.11:g.143426245_143426246dup , CM000665.1:g.143426245_143426246dup GRCh37
NC_000003.10:g.144908935_144908936dup NCBI36
NG_017077.1:g.146130_146131dup
NG_017077.2:g.146130_146131dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-14095_534-14094dup MANE Select ENSP00000320246.6:n.534-14095_534-14094dup
ENST00000316549.10:c.534-14095_534-14094dup ENSP00000320246.6:n.534-14095_534-14094dup
ENST00000474727.2:c.*145-14095_*145-14094dup ENSP00000419090.2:n.*145-14095_*145-14094dup
NM_173653.3:c.534-14095_534-14094dup NP_775924.1:n.534-14095_534-14094dup
XM_011512704.1:c.534-14095_534-14094dup XP_011511006.1:n.534-14095_534-14094dup
XM_011512704.3:c.534-14095_534-14094dup XP_011511006.1:n.534-14095_534-14094dup
XM_017006202.2:c.534-14095_534-14094dup XP_016861691.1:n.534-14095_534-14094dup
XM_017006203.1:c.183-14095_183-14094dup XP_016861692.1:n.183-14095_183-14094dup
NM_173653.4:c.534-14095_534-14094dup MANE Select NP_775924.1:n.534-14095_534-14094dup
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