Canonical Allele Identifier: CA874145129
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs1434251734

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010204_25010207del , CM000685.2:g.25010204_25010207del GRCh38
NC_000023.10:g.25028321_25028324del , CM000685.1:g.25028321_25028324del GRCh37
NC_000023.9:g.24938242_24938245del NCBI36
NG_008281.1:g.10750_10753del

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+61_1119+64del MANE Select ENSP00000368332.4:n.1119+61_1119+64del
ENST00000379044.4:c.1119+61_1119+64del ENSP00000368332.4:n.1119+61_1119+64del
NM_139058.2:c.1119+61_1119+64del NP_620689.1:n.1119+61_1119+64del
NM_139058.3:c.1119+61_1119+64del MANE Select NP_620689.1:n.1119+61_1119+64del