Canonical Allele Identifier: CA313926372

Gene: ASXL1

Linked Data

• dbSNP Id: rs957498028
• gnomAD v2: 20-31024566-A-G
• gnomAD v3: 20-32436763-A-G
• gnomAD v4: 20-32436763-A-G
• MyVariant Identifiers: chr20:g.31024566A>G (hg19) ; chr20:g.32436763A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436763A>G , CM000682.2:g.32436763A>G	GRCh38
NC_000020.10:g.31024566A>G , CM000682.1:g.31024566A>G	GRCh37
NC_000020.9:g.30488227A>G	NCBI36
NG_027868.1:g.83420A>G , LRG_630:g.83420A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4051A>G MANE Select	ENSP00000364839.4:p.Thr1351Ala
ENST00000646985.1:c.3868A>G	ENSP00000495053.1:p.Thr1290Ala
ENST00000647223.1:n.6404A>G
ENST00000651418.1:c.1870-1667A>G	ENSP00000499150.1:n.1870-1667A>G
ENST00000306058.9:c.4036A>G	ENSP00000305119.5:p.Thr1346Ala
ENST00000375687.8:c.4051A>G	ENSP00000364839.4:p.Thr1351Ala
ENST00000613218.4:c.4051A>G	ENSP00000480487.1:p.Thr1351Ala
ENST00000620121.4:c.4051A>G	ENSP00000481978.1:p.Thr1351Ala
NM_015338.5:c.4051A>G , LRG_630t1:c.4051A>G	NP_056153.2:p.Thr1351Ala
XM_006723727.2:c.4048A>G	XP_006723790.1:p.Thr1350Ala
XM_006723728.2:c.4021A>G	XP_006723791.1:p.Thr1341Ala
XM_006723730.2:c.3967A>G	XP_006723793.1:p.Thr1323Ala
XM_006723732.2:c.3868A>G	XP_006723795.1:p.Thr1290Ala
XM_006723733.1:c.3367A>G	XP_006723796.1:p.Thr1123Ala
XM_011528647.1:c.4315A>G	XP_011526949.1:p.Thr1439Ala
XM_011528648.1:c.4312A>G	XP_011526950.1:p.Thr1438Ala
XM_011528649.1:c.4231A>G	XP_011526951.1:p.Thr1411Ala
XM_011528650.1:c.4162A>G	XP_011526952.1:p.Thr1388Ala
XM_011528651.1:c.4030A>G	XP_011526953.1:p.Thr1344Ala
XM_011528652.1:c.3967A>G	XP_011526954.1:p.Thr1323Ala
NM_001363734.1:c.3868A>G	NP_001350663.1:p.Thr1290Ala
XM_006723727.3:c.4048A>G	XP_006723790.1:p.Thr1350Ala
XM_006723728.3:c.4021A>G	XP_006723791.1:p.Thr1341Ala
XM_006723730.4:c.3967A>G	XP_006723793.1:p.Thr1323Ala
XM_011528648.3:c.4312A>G	XP_011526950.1:p.Thr1438Ala
XM_011528652.2:c.3967A>G	XP_011526954.1:p.Thr1323Ala
XM_017027704.1:c.3967A>G	XP_016883193.1:p.Thr1323Ala
XM_017027705.1:c.3967A>G	XP_016883194.1:p.Thr1323Ala
XM_017027706.1:c.3898A>G	XP_016883195.1:p.Thr1300Ala
NM_015338.6:c.4051A>G MANE Select	NP_056153.2:p.Thr1351Ala