Canonical Allele Identifier: CA641364618
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs1569395209
gnomAD v2: X-25030938-A-ATT
gnomAD v3: X-25012821-A-ATT
gnomAD v4: X-25012821-A-ATT
MyVariant Identifiers: chrX:g.25030938_25030939insTT (hg19) chrX:g.25012821_25012822insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012821_25012822insTT , CM000685.2:g.25012821_25012822insTT GRCh38
NC_000023.10:g.25030938_25030939insTT , CM000685.1:g.25030938_25030939insTT GRCh37
NC_000023.9:g.24940859_24940860insTT NCBI36
NG_008281.1:g.8127_8128insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1073+100_1073+101insAA MANE Select ENSP00000368332.4:n.1073+100_1073+101insAA
ENST00000379044.4:c.1073+100_1073+101insAA ENSP00000368332.4:n.1073+100_1073+101insAA
NM_139058.2:c.1073+100_1073+101insAA NP_620689.1:n.1073+100_1073+101insAA
NM_139058.3:c.1073+100_1073+101insAA MANE Select NP_620689.1:n.1073+100_1073+101insAA
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