Canonical Allele Identifier: CA410603018

Gene: U2AF1

Linked Data

• MyVariant Identifiers: chr21:g.43094490A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43094490A>T , CM000683.2:g.43094490A>T	GRCh38
NG_029455.1:g.18089T>A , LRG_615:g.18089T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291552.9:c.556T>A MANE Select	ENSP00000291552.4:p.Tyr186Asn
ENST00000291552.8:c.556T>A	ENSP00000291552.4:p.Tyr186Asn
ENST00000380276.6:c.556T>A	ENSP00000369629.2:p.Tyr186Asn
ENST00000398137.5:c.337T>A	ENSP00000381205.1:p.Tyr113Asn
ENST00000459639.5:c.337T>A	ENSP00000418705.1:p.Tyr113Asn
ENST00000464750.5:c.*395T>A	ENSP00000420672.1:n.*395T>A
ENST00000471250.5:n.1363T>A
ENST00000475639.5:n.4381T>A
ENST00000478282.1:n.1810T>A
ENST00000486519.5:n.603T>A
NM_001025203.1:c.556T>A , LRG_615t1:c.556T>A	NP_001020374.1:p.Tyr186Asn
NM_001025204.1:c.337T>A	NP_001020375.1:p.Tyr113Asn
NM_006758.2:c.556T>A , LRG_615t2:c.556T>A	NP_006749.1:p.Tyr186Asn
XM_011529743.1:c.457T>A	XP_011528045.1:p.Tyr153Asn
XM_011529743.3:c.457T>A	XP_011528045.1:p.Tyr153Asn
XM_017028468.2:c.457T>A	XP_016883957.1:p.Tyr153Asn
XM_024452129.1:c.337T>A	XP_024307897.1:p.Tyr113Asn
XM_024452130.1:c.337T>A	XP_024307898.1:p.Tyr113Asn
XM_024452131.1:c.337T>A	XP_024307899.1:p.Tyr113Asn
NM_001025204.2:c.337T>A	NP_001020375.1:p.Tyr113Asn
NM_006758.3:c.556T>A MANE Select	NP_006749.1:p.Tyr186Asn