Canonical Allele Identifier: CA868684272
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs1261468784
gnomAD v3: 9-93953317-TGCCGGTCGGC-T
gnomAD v4: 9-93953317-TGCCGGTCGGC-T
MyVariant Identifiers: chr9:g.96715600_96715609del (hg19) chr9:g.93953318_93953327del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93953324_93953333del , CM000671.2:g.93953324_93953333del GRCh38
NC_000009.11:g.96715606_96715615del , CM000671.1:g.96715606_96715615del GRCh37
NC_000009.10:g.95755427_95755436del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.224-140_224-131del MANE Select ENSP00000253968.5:n.224-140_224-131del
ENST00000253968.10:c.224-140_224-131del ENSP00000253968.5:n.224-140_224-131del
ENST00000401724.1:c.-379_-370del ENSP00000385613.1:n.-379_-370del
NM_021570.3:c.224-140_224-131del NP_067545.3:n.224-140_224-131del
NM_021570.4:c.224-140_224-131del MANE Select NP_067545.3:n.224-140_224-131del
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