Canonical Allele Identifier: CA1055218

Gene: RBM8A LIX1L-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.145927445C>T , CM000663.2:g.145927445C>T	GRCh38
NC_000001.10:g.145507648G>A , CM000663.1:g.145507648G>A	GRCh37
NC_000001.9:g.144219005G>A	NCBI36
NG_032654.2:g.5092G>A , LRG_574:g.5092G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005105.5:c.-19G>A (RBM8A) MANE Select	NP_005096.1:n.-19G>A
ENST00000583313.7:c.-19G>A (RBM8A) MANE Select	ENSP00000463058.2:n.-19G>A
NM_005105.4:c.-19G>A , LRG_574t1:c.-19G>A (RBM8A)	NP_005096.1:n.-19G>A
NR_147182.1:n.498C>T (LIX1L-AS1)
ENST00000369307.4:c.-19G>A (RBM8A)	ENSP00000358313.3:n.-19G>A
ENST00000484825.1:n.51G>A (RBM8A)
ENST00000498663.5:n.51G>A (RBM8A)
ENST00000583313.6:c.-19G>A (RBM8A)	ENSP00000463058.1:n.-19G>A
ENST00000625258.1:c.-30+156C>T	ENSP00000487094.1:n.-30+156C>T
ENST00000630636.1:n.188C>T
ENST00000632555.1:c.-19G>A (RBM8A)	ENSP00000488265.1:n.-19G>A
ENST00000634161.1:n.118G>A (RBM8A)
ENST00000691760.1:c.-19G>A (RBM8A)	ENSP00000510519.1:n.-19G>A
ENST00000692065.1:n.20G>A (RBM8A)