Canonical Allele Identifier: CA2420210079
Gene: ARX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015520T= , CM000685.2:g.25015520T= GRCh38
NC_000023.10:g.25033637T= , CM000685.1:g.25033637T= GRCh37
NC_000023.9:g.24943558T= NCBI36
NG_008281.1:g.5429A=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.196+22A= MANE Select ENSP00000368332.4:n.196+22A=
ENST00000379044.4:c.196+22A= ENSP00000368332.4:n.196+22A=
NM_139058.2:c.196+22A= NP_620689.1:n.196+22A=
NM_139058.3:c.196+22A= MANE Select NP_620689.1:n.196+22A=
Search 100 bp 5'
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