Canonical Allele Identifier: CA915941068
Community Standard Title: NM_005105.5(RBM8A):c.206-13C>A
Gene: RBM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145926631G>T , CM000663.2:g.145926631G>T GRCh38
NC_000001.10:g.145508462C>A , CM000663.1:g.145508462C>A GRCh37
NC_000001.9:g.144219819C>A NCBI36
NG_032654.2:g.5906C>A , LRG_574:g.5906C>A

Transcript Alleles

HGVS Amino-acid Change
NM_005105.5:c.206-13C>A MANE Select NP_005096.1:n.206-13C>A
ENST00000583313.7:c.206-13C>A MANE Select ENSP00000463058.2:n.206-13C>A
NM_005105.4:c.206-13C>A , LRG_574t1:c.206-13C>A NP_005096.1:n.206-13C>A
ENST00000369307.4:c.203-13C>A ENSP00000358313.3:n.203-13C>A
ENST00000484825.1:n.406-13C>A
ENST00000498663.5:n.583C>A
ENST00000583313.6:c.206-13C>A ENSP00000463058.1:n.206-13C>A
ENST00000632555.1:c.206-13C>A ENSP00000488265.1:n.206-13C>A
ENST00000634130.1:n.111C>A
ENST00000691760.1:c.206-13C>A ENSP00000510519.1:n.206-13C>A
ENST00000692065.1:n.552C>A