Canonical Allele Identifier: CA408562911

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023882C>A (hg19) ; chr20:g.32436079C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436079C>A , CM000682.2:g.32436079C>A	GRCh38
NC_000020.10:g.31023882C>A , CM000682.1:g.31023882C>A	GRCh37
NC_000020.9:g.30487543C>A	NCBI36
NG_027868.1:g.82736C>A , LRG_630:g.82736C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3367C>A MANE Select	ENSP00000364839.4:p.Pro1123Thr
ENST00000646985.1:c.3184C>A	ENSP00000495053.1:p.Pro1062Thr
ENST00000647223.1:n.5720C>A
ENST00000651418.1:c.1869+1498C>A	ENSP00000499150.1:n.1869+1498C>A
ENST00000306058.9:c.3352C>A	ENSP00000305119.5:p.Pro1118Thr
ENST00000375687.8:c.3367C>A	ENSP00000364839.4:p.Pro1123Thr
ENST00000613218.4:c.3367C>A	ENSP00000480487.1:p.Pro1123Thr
ENST00000620121.4:c.3367C>A	ENSP00000481978.1:p.Pro1123Thr
NM_015338.5:c.3367C>A , LRG_630t1:c.3367C>A	NP_056153.2:p.Pro1123Thr
XM_006723727.2:c.3364C>A	XP_006723790.1:p.Pro1122Thr
XM_006723728.2:c.3337C>A	XP_006723791.1:p.Pro1113Thr
XM_006723730.2:c.3283C>A	XP_006723793.1:p.Pro1095Thr
XM_006723732.2:c.3184C>A	XP_006723795.1:p.Pro1062Thr
XM_006723733.1:c.2683C>A	XP_006723796.1:p.Pro895Thr
XM_011528647.1:c.3631C>A	XP_011526949.1:p.Pro1211Thr
XM_011528648.1:c.3628C>A	XP_011526950.1:p.Pro1210Thr
XM_011528649.1:c.3547C>A	XP_011526951.1:p.Pro1183Thr
XM_011528650.1:c.3478C>A	XP_011526952.1:p.Pro1160Thr
XM_011528651.1:c.3346C>A	XP_011526953.1:p.Pro1116Thr
XM_011528652.1:c.3283C>A	XP_011526954.1:p.Pro1095Thr
NM_001363734.1:c.3184C>A	NP_001350663.1:p.Pro1062Thr
XM_006723727.3:c.3364C>A	XP_006723790.1:p.Pro1122Thr
XM_006723728.3:c.3337C>A	XP_006723791.1:p.Pro1113Thr
XM_006723730.4:c.3283C>A	XP_006723793.1:p.Pro1095Thr
XM_011528648.3:c.3628C>A	XP_011526950.1:p.Pro1210Thr
XM_011528652.2:c.3283C>A	XP_011526954.1:p.Pro1095Thr
XM_017027704.1:c.3283C>A	XP_016883193.1:p.Pro1095Thr
XM_017027705.1:c.3283C>A	XP_016883194.1:p.Pro1095Thr
XM_017027706.1:c.3214C>A	XP_016883195.1:p.Pro1072Thr
NM_015338.6:c.3367C>A MANE Select	NP_056153.2:p.Pro1123Thr