Canonical Allele Identifier: CA1144228958
Gene: RBM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145925920G= , CM000663.2:g.145925920G= GRCh38
NC_000001.10:g.145509173C= , CM000663.1:g.145509173C= GRCh37
NC_000001.9:g.144220530C= NCBI36
NG_032654.2:g.6617C= , LRG_574:g.6617C=

Transcript Alleles

HGVS Amino-acid Change
NM_005105.5:c.487C= MANE Select NP_005096.1:p.Arg163=
ENST00000583313.7:c.487C= MANE Select ENSP00000463058.2:p.Arg163=
NM_005105.4:c.487C= , LRG_574t1:c.487C= NP_005096.1:p.Arg163=
ENST00000369307.4:c.484C= ENSP00000358313.3:p.Arg162=
ENST00000583313.6:c.487C= ENSP00000463058.1:p.Arg163=
ENST00000632040.1:c.282C=
ENST00000632555.1:c.487C= ENSP00000488265.1:p.Arg163=
ENST00000633781.1:c.282C=
ENST00000634130.1:n.405C=
ENST00000691760.1:c.487C= ENSP00000510519.1:p.Arg163=
ENST00000692065.1:n.846C=