Canonical Allele Identifier: CA2420208082
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010400_25010402delinsGGT , CM000685.2:g.25010400_25010402delinsGGT GRCh38
NC_000023.10:g.25028517_25028519delinsGGT , CM000685.1:g.25028517_25028519delinsGGT GRCh37
NC_000023.9:g.24938438_24938440delinsGGT NCBI36
NG_008281.1:g.10547_10549delinsACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1074-97_1074-95delinsACC MANE Select ENSP00000368332.4:n.1074-97_1074-95delinsACC
ENST00000379044.4:c.1074-97_1074-95delinsACC ENSP00000368332.4:n.1074-97_1074-95delinsACC
NM_139058.2:c.1074-97_1074-95delinsACC NP_620689.1:n.1074-97_1074-95delinsACC
NM_139058.3:c.1074-97_1074-95delinsACC MANE Select NP_620689.1:n.1074-97_1074-95delinsACC