Canonical Allele Identifier: CA369161896

Gene: RBM28

Linked Data

• MyVariant Identifiers: chr7:g.127970950G>T (hg19) ; chr7:g.128330897G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128330897G>T , CM000669.2:g.128330897G>T	GRCh38
NC_000007.13:g.127970950G>T , CM000669.1:g.127970950G>T	GRCh37
NC_000007.12:g.127758186G>T	NCBI36
NG_015802.1:g.18013C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000223073.6:c.1051C>A MANE Select	ENSP00000223073.1:p.Leu351Ile
ENST00000415472.6:c.628C>A	ENSP00000390517.2:p.Leu210Ile
ENST00000487602.5:c.468C>A
NM_001166135.1:c.628C>A	NP_001159607.1:p.Leu210Ile
NM_018077.2:c.1051C>A	NP_060547.2:p.Leu351Ile
XM_011516370.1:c.1153C>A	XP_011514672.1:p.Leu385Ile
XM_011516371.1:c.57C>A	XP_011514673.1:p.Asn19Lys
XR_927487.1:n.1273C>A
XM_011516370.3:c.1153C>A	XP_011514672.1:p.Leu385Ile
XM_017012389.1:c.1153C>A	XP_016867878.1:p.Leu385Ile
XM_017012390.1:c.1051C>A	XP_016867879.1:p.Leu351Ile
XR_001744830.1:n.1275C>A
NM_001166135.2:c.628C>A	NP_001159607.1:p.Leu210Ile
NM_018077.3:c.1051C>A MANE Select	NP_060547.2:p.Leu351Ile