Canonical Allele Identifier: CA2420208008
Gene: ARX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010201C= , CM000685.2:g.25010201C= GRCh38
NC_000023.10:g.25028318C= , CM000685.1:g.25028318C= GRCh37
NC_000023.9:g.24938239C= NCBI36
NG_008281.1:g.10748G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+59G= MANE Select ENSP00000368332.4:n.1119+59G=
ENST00000379044.4:c.1119+59G= ENSP00000368332.4:n.1119+59G=
NM_139058.2:c.1119+59G= NP_620689.1:n.1119+59G=
NM_139058.3:c.1119+59G= MANE Select NP_620689.1:n.1119+59G=
Search 100 bp 5'
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