Canonical Allele Identifier: CA408563052

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023947T>A (hg19) ; chr20:g.32436144T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436144T>A , CM000682.2:g.32436144T>A	GRCh38
NC_000020.10:g.31023947T>A , CM000682.1:g.31023947T>A	GRCh37
NC_000020.9:g.30487608T>A	NCBI36
NG_027868.1:g.82801T>A , LRG_630:g.82801T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3432T>A MANE Select	ENSP00000364839.4:p.His1144Gln
ENST00000646985.1:c.3249T>A	ENSP00000495053.1:p.His1083Gln
ENST00000647223.1:n.5785T>A
ENST00000651418.1:c.1869+1563T>A	ENSP00000499150.1:n.1869+1563T>A
ENST00000306058.9:c.3417T>A	ENSP00000305119.5:p.His1139Gln
ENST00000375687.8:c.3432T>A	ENSP00000364839.4:p.His1144Gln
ENST00000613218.4:c.3432T>A	ENSP00000480487.1:p.His1144Gln
ENST00000620121.4:c.3432T>A	ENSP00000481978.1:p.His1144Gln
NM_015338.5:c.3432T>A , LRG_630t1:c.3432T>A	NP_056153.2:p.His1144Gln
XM_006723727.2:c.3429T>A	XP_006723790.1:p.His1143Gln
XM_006723728.2:c.3402T>A	XP_006723791.1:p.His1134Gln
XM_006723730.2:c.3348T>A	XP_006723793.1:p.His1116Gln
XM_006723732.2:c.3249T>A	XP_006723795.1:p.His1083Gln
XM_006723733.1:c.2748T>A	XP_006723796.1:p.His916Gln
XM_011528647.1:c.3696T>A	XP_011526949.1:p.His1232Gln
XM_011528648.1:c.3693T>A	XP_011526950.1:p.His1231Gln
XM_011528649.1:c.3612T>A	XP_011526951.1:p.His1204Gln
XM_011528650.1:c.3543T>A	XP_011526952.1:p.His1181Gln
XM_011528651.1:c.3411T>A	XP_011526953.1:p.His1137Gln
XM_011528652.1:c.3348T>A	XP_011526954.1:p.His1116Gln
NM_001363734.1:c.3249T>A	NP_001350663.1:p.His1083Gln
XM_006723727.3:c.3429T>A	XP_006723790.1:p.His1143Gln
XM_006723728.3:c.3402T>A	XP_006723791.1:p.His1134Gln
XM_006723730.4:c.3348T>A	XP_006723793.1:p.His1116Gln
XM_011528648.3:c.3693T>A	XP_011526950.1:p.His1231Gln
XM_011528652.2:c.3348T>A	XP_011526954.1:p.His1116Gln
XM_017027704.1:c.3348T>A	XP_016883193.1:p.His1116Gln
XM_017027705.1:c.3348T>A	XP_016883194.1:p.His1116Gln
XM_017027706.1:c.3279T>A	XP_016883195.1:p.His1093Gln
NM_015338.6:c.3432T>A MANE Select	NP_056153.2:p.His1144Gln