Canonical Allele Identifier: CA342126755
Gene: RBM8A HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_005105.5:c.487C>G MANE Select NP_005096.1:p.Arg163Gly
ENST00000583313.7:c.487C>G MANE Select ENSP00000463058.2:p.Arg163Gly
NM_005105.4:c.487C>G , LRG_574t1:c.487C>G NP_005096.1:p.Arg163Gly
ENST00000369307.4:c.484C>G ENSP00000358313.3:p.Arg162Gly
ENST00000583313.6:c.487C>G ENSP00000463058.1:p.Arg163Gly
ENST00000632040.1:c.282C>G
ENST00000632555.1:c.487C>G ENSP00000488265.1:p.Arg163Gly
ENST00000633781.1:c.282C>G
ENST00000634130.1:n.405C>G
ENST00000691760.1:c.487C>G ENSP00000510519.1:p.Arg163Gly
ENST00000692065.1:n.846C>G