Canonical Allele Identifier: CA510467024

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023689G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435886G>T , CM000682.2:g.32435886G>T	GRCh38
NC_000020.10:g.31023689G>T , CM000682.1:g.31023689G>T	GRCh37
NC_000020.9:g.30487350G>T	NCBI36
NG_027868.1:g.82543G>T , LRG_630:g.82543G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3174G>T MANE Select	ENSP00000364839.4:p.Gly1058=
ENST00000646985.1:c.2991G>T	ENSP00000495053.1:p.Gly997=
ENST00000647223.1:n.5527G>T
ENST00000651418.1:c.1869+1305G>T	ENSP00000499150.1:n.1869+1305G>T
ENST00000306058.9:c.3159G>T	ENSP00000305119.5:p.Gly1053=
ENST00000375687.8:c.3174G>T	ENSP00000364839.4:p.Gly1058=
ENST00000613218.4:c.3174G>T	ENSP00000480487.1:p.Gly1058=
ENST00000620121.4:c.3174G>T	ENSP00000481978.1:p.Gly1058=
NM_015338.5:c.3174G>T , LRG_630t1:c.3174G>T	NP_056153.2:p.Gly1058=
XM_006723727.2:c.3171G>T	XP_006723790.1:p.Gly1057=
XM_006723728.2:c.3144G>T	XP_006723791.1:p.Gly1048=
XM_006723730.2:c.3090G>T	XP_006723793.1:p.Gly1030=
XM_006723732.2:c.2991G>T	XP_006723795.1:p.Gly997=
XM_006723733.1:c.2490G>T	XP_006723796.1:p.Gly830=
XM_011528647.1:c.3438G>T	XP_011526949.1:p.Gly1146=
XM_011528648.1:c.3435G>T	XP_011526950.1:p.Gly1145=
XM_011528649.1:c.3354G>T	XP_011526951.1:p.Gly1118=
XM_011528650.1:c.3285G>T	XP_011526952.1:p.Gly1095=
XM_011528651.1:c.3153G>T	XP_011526953.1:p.Gly1051=
XM_011528652.1:c.3090G>T	XP_011526954.1:p.Gly1030=
NM_001363734.1:c.2991G>T	NP_001350663.1:p.Gly997=
XM_006723727.3:c.3171G>T	XP_006723790.1:p.Gly1057=
XM_006723728.3:c.3144G>T	XP_006723791.1:p.Gly1048=
XM_006723730.4:c.3090G>T	XP_006723793.1:p.Gly1030=
XM_011528648.3:c.3435G>T	XP_011526950.1:p.Gly1145=
XM_011528652.2:c.3090G>T	XP_011526954.1:p.Gly1030=
XM_017027704.1:c.3090G>T	XP_016883193.1:p.Gly1030=
XM_017027705.1:c.3090G>T	XP_016883194.1:p.Gly1030=
XM_017027706.1:c.3021G>T	XP_016883195.1:p.Gly1007=
NM_015338.6:c.3174G>T MANE Select	NP_056153.2:p.Gly1058=