Canonical Allele Identifier: CA85301859
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs67386185
gnomAD v2: 3-143426211-T-TAC
gnomAD v3: 3-143707369-T-TAC
gnomAD v4: 3-143707369-T-TAC
MyVariant Identifiers: chr3:g.143426243_143426244insAC (hg19) chr3:g.143426217_143426218insAC (hg19) chr3:g.143426213_143426214insAC (hg19) chr3:g.143426211_143426212insAC (hg19) chr3:g.143707401_143707402insAC (hg38) chr3:g.143707375_143707376insAC (hg38) chr3:g.143707371_143707372insAC (hg38) chr3:g.143707369_143707370insAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707400_143707401dup , CM000665.2:g.143707400_143707401dup GRCh38
NC_000003.11:g.143426242_143426243dup , CM000665.1:g.143426242_143426243dup GRCh37
NC_000003.10:g.144908932_144908933dup NCBI36
NG_017077.1:g.146161_146162dup
NG_017077.2:g.146161_146162dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-14064_534-14063dup MANE Select ENSP00000320246.6:n.534-14064_534-14063dup
ENST00000316549.10:c.534-14064_534-14063dup ENSP00000320246.6:n.534-14064_534-14063dup
ENST00000474727.2:c.*145-14064_*145-14063dup ENSP00000419090.2:n.*145-14064_*145-14063dup
NM_173653.3:c.534-14064_534-14063dup NP_775924.1:n.534-14064_534-14063dup
XM_011512704.1:c.534-14064_534-14063dup XP_011511006.1:n.534-14064_534-14063dup
XM_011512704.3:c.534-14064_534-14063dup XP_011511006.1:n.534-14064_534-14063dup
XM_017006202.2:c.534-14064_534-14063dup XP_016861691.1:n.534-14064_534-14063dup
XM_017006203.1:c.183-14064_183-14063dup XP_016861692.1:n.183-14064_183-14063dup
NM_173653.4:c.534-14064_534-14063dup MANE Select NP_775924.1:n.534-14064_534-14063dup
Search 100 bp 5'
Search 100 bp 3'