Canonical Allele Identifier: CA10482250
Gene: RADX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106633242T>C , CM000685.2:g.106633242T>C GRCh38
NC_000023.10:g.105876472T>C , CM000685.1:g.105876472T>C GRCh37
NC_000023.9:g.105763128T>C NCBI36
NG_021317.1:g.26313T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372548.9:c.1293T>C MANE Select ENSP00000361628.4:p.Asn431=
ENST00000372544.6:c.1293T>C ENSP00000361623.2:p.Asn431=
ENST00000372548.8:c.1293T>C ENSP00000361628.4:p.Asn431=
ENST00000421550.1:c.717T>C ENSP00000405866.1:p.Asn239=
ENST00000461251.5:c.1293T>C ENSP00000432238.1:p.Asn431=
NM_001184782.1:c.1293T>C NP_001171711.1:p.Asn431=
NM_018015.5:c.1293T>C NP_060485.4:p.Asn431=
XM_011530978.1:c.1293T>C XP_011529280.1:p.Asn431=
XR_001755707.2:n.1417T>C
NM_018015.6:c.1293T>C MANE Select NP_060485.4:p.Asn431=
NM_001184782.2:c.1293T>C NP_001171711.1:p.Asn431=