Canonical Allele Identifier: CA410603191

Gene: U2AF1

Linked Data

• MyVariant Identifiers: chr21:g.43094653A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43094653A>C , CM000683.2:g.43094653A>C	GRCh38
NG_029455.1:g.17926T>G , LRG_615:g.17926T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291552.9:c.482+2T>G MANE Select	ENSP00000291552.4:n.482+2T>G
ENST00000291552.8:c.482+2T>G	ENSP00000291552.4:n.482+2T>G
ENST00000380276.6:c.482+2T>G	ENSP00000369629.2:n.482+2T>G
ENST00000398137.5:c.263+2T>G	ENSP00000381205.1:n.263+2T>G
ENST00000459639.5:c.263+2T>G	ENSP00000418705.1:n.263+2T>G
ENST00000464750.5:c.*321+2T>G	ENSP00000420672.1:n.*321+2T>G
ENST00000471250.5:n.1289+2T>G
ENST00000475639.5:n.4307+2T>G
ENST00000478282.1:n.1736+2T>G
ENST00000486519.5:n.529+2T>G
NM_001025203.1:c.482+2T>G , LRG_615t1:c.482+2T>G	NP_001020374.1:n.482+2T>G
NM_001025204.1:c.263+2T>G	NP_001020375.1:n.263+2T>G
NM_006758.2:c.482+2T>G , LRG_615t2:c.482+2T>G	NP_006749.1:n.482+2T>G
XM_011529743.1:c.383+2T>G	XP_011528045.1:n.383+2T>G
XM_011529743.3:c.383+2T>G	XP_011528045.1:n.383+2T>G
XM_017028468.2:c.383+2T>G	XP_016883957.1:n.383+2T>G
XM_024452129.1:c.263+2T>G	XP_024307897.1:n.263+2T>G
XM_024452130.1:c.263+2T>G	XP_024307898.1:n.263+2T>G
XM_024452131.1:c.263+2T>G	XP_024307899.1:n.263+2T>G
NM_001025204.2:c.263+2T>G	NP_001020375.1:n.263+2T>G
NM_006758.3:c.482+2T>G MANE Select	NP_006749.1:n.482+2T>G