Canonical Allele Identifier: CA410603069

Gene: U2AF1

Linked Data

• MyVariant Identifiers: chr21:g.43094516A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43094516A>T , CM000683.2:g.43094516A>T	GRCh38
NG_029455.1:g.18063T>A , LRG_615:g.18063T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291552.9:c.530T>A MANE Select	ENSP00000291552.4:p.Ile177Asn
ENST00000291552.8:c.530T>A	ENSP00000291552.4:p.Ile177Asn
ENST00000380276.6:c.530T>A	ENSP00000369629.2:p.Ile177Asn
ENST00000398137.5:c.311T>A	ENSP00000381205.1:p.Ile104Asn
ENST00000459639.5:c.311T>A	ENSP00000418705.1:p.Ile104Asn
ENST00000464750.5:c.*369T>A	ENSP00000420672.1:n.*369T>A
ENST00000471250.5:n.1337T>A
ENST00000475639.5:n.4355T>A
ENST00000478282.1:n.1784T>A
ENST00000486519.5:n.577T>A
NM_001025203.1:c.530T>A , LRG_615t1:c.530T>A	NP_001020374.1:p.Ile177Asn
NM_001025204.1:c.311T>A	NP_001020375.1:p.Ile104Asn
NM_006758.2:c.530T>A , LRG_615t2:c.530T>A	NP_006749.1:p.Ile177Asn
XM_011529743.1:c.431T>A	XP_011528045.1:p.Ile144Asn
XM_011529743.3:c.431T>A	XP_011528045.1:p.Ile144Asn
XM_017028468.2:c.431T>A	XP_016883957.1:p.Ile144Asn
XM_024452129.1:c.311T>A	XP_024307897.1:p.Ile104Asn
XM_024452130.1:c.311T>A	XP_024307898.1:p.Ile104Asn
XM_024452131.1:c.311T>A	XP_024307899.1:p.Ile104Asn
NM_001025204.2:c.311T>A	NP_001020375.1:p.Ile104Asn
NM_006758.3:c.530T>A MANE Select	NP_006749.1:p.Ile177Asn