Canonical Allele Identifier: CA433677797

Gene: RBM5 RBM6

Linked Data

• MyVariant Identifiers: chr3:g.50129549C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50092116C>A , CM000665.2:g.50092116C>A	GRCh38
NC_000003.11:g.50129549C>A , CM000665.1:g.50129549C>A	GRCh37
NC_000003.10:g.50104553C>A	NCBI36
NG_030403.1:g.8209C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347869.8:c.91C>A (RBM5) MANE Select	ENSP00000343054.3:p.Arg31=
ENST00000347869.7:c.91C>A (RBM5)	ENSP00000343054.3:p.Arg31=
ENST00000404526.6:c.91C>A (RBM5)	ENSP00000384872.2:p.Arg31=
ENST00000417905.1:c.91C>A (RBM5)	ENSP00000406119.1:p.Arg31=
ENST00000433556.6:n.220C>A (RBM5)
ENST00000434592.5:c.*1111C>A (RBM6)	ENSP00000399942.1:n.*1111C>A
ENST00000437500.5:c.91C>A (RBM5)	ENSP00000394622.1:p.Arg31=
ENST00000438369.5:c.91C>A (RBM5)	ENSP00000414218.1:p.Arg31=
ENST00000441305.5:c.91C>A (RBM5)	ENSP00000390711.1:p.Arg31=
ENST00000464087.6:n.211C>A (RBM5)
ENST00000469838.5:c.91C>A (RBM5)	ENSP00000419534.1:p.Arg31=
ENST00000492472.1:n.199C>A (RBM5)
NM_005778.3:c.91C>A (RBM5)	NP_005769.1:p.Arg31=
NR_036627.2:n.266C>A (RBM5)
XM_006712917.1:c.91C>A (RBM5)	XP_006712980.1:p.Arg31=
XM_011533261.1:c.91C>A (RBM5)	XP_011531563.1:p.Arg31=
XM_011533262.1:c.91C>A (RBM5)	XP_011531564.1:p.Arg31=
XR_427245.1:n.266C>A (RBM5)
XM_006712917.2:c.91C>A (RBM5)	XP_006712980.1:p.Arg31=
XM_011533261.2:c.91C>A (RBM5)	XP_011531563.1:p.Arg31=
XM_011533262.2:c.91C>A (RBM5)	XP_011531564.1:p.Arg31=
XM_017005503.1:c.91C>A (RBM5)	XP_016860992.1:p.Arg31=
XM_017005504.2:c.91C>A (RBM5)	XP_016860993.1:p.Arg31=
XM_017005505.1:c.-590C>A (RBM5)	XP_016860994.1:n.-590C>A
XM_024453289.1:c.-516C>A (RBM5)	XP_024309057.1:n.-516C>A
XM_024453290.1:c.-3547C>A (RBM5)	XP_024309058.1:n.-3547C>A
XR_427245.2:n.255C>A (RBM5)
NM_005778.4:c.91C>A (RBM5) MANE Select	NP_005769.1:p.Arg31=
NR_036627.3:n.255C>A (RBM5)