Canonical Allele Identifier: CA2420206979

Gene: ARX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25007083C= , CM000685.2:g.25007083C=	GRCh38
NC_000023.10:g.25025200C= , CM000685.1:g.25025200C=	GRCh37
NC_000023.9:g.24935121C=	NCBI36
NG_008281.1:g.13866G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379044.5:c.1448+28G= MANE Select	ENSP00000368332.4:n.1448+28G=
ENST00000637993.1:c.61+28G=
ENST00000379044.4:c.1448+28G=	ENSP00000368332.4:n.1448+28G=
NM_139058.2:c.1448+28G=	NP_620689.1:n.1448+28G=
NM_139058.3:c.1448+28G= MANE Select	NP_620689.1:n.1448+28G=