Canonical Allele Identifier: CA2420206966
Gene: ARX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007051C= , CM000685.2:g.25007051C= GRCh38
NC_000023.10:g.25025168C= , CM000685.1:g.25025168C= GRCh37
NC_000023.9:g.24935089C= NCBI36
NG_008281.1:g.13898G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1448+60G= MANE Select ENSP00000368332.4:n.1448+60G=
ENST00000637993.1:c.61+60G=
ENST00000379044.4:c.1448+60G= ENSP00000368332.4:n.1448+60G=
NM_139058.2:c.1448+60G= NP_620689.1:n.1448+60G=
NM_139058.3:c.1448+60G= MANE Select NP_620689.1:n.1448+60G=
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