Canonical Allele Identifier: CA408564427

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024608G>T (hg19) ; chr20:g.32436805G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436805G>T , CM000682.2:g.32436805G>T	GRCh38
NC_000020.10:g.31024608G>T , CM000682.1:g.31024608G>T	GRCh37
NC_000020.9:g.30488269G>T	NCBI36
NG_027868.1:g.83462G>T , LRG_630:g.83462G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4093G>T MANE Select	ENSP00000364839.4:p.Gly1365Cys
ENST00000646985.1:c.3910G>T	ENSP00000495053.1:p.Gly1304Cys
ENST00000647223.1:n.6446G>T
ENST00000651418.1:c.1870-1625G>T	ENSP00000499150.1:n.1870-1625G>T
ENST00000306058.9:c.4078G>T	ENSP00000305119.5:p.Gly1360Cys
ENST00000375687.8:c.4093G>T	ENSP00000364839.4:p.Gly1365Cys
ENST00000613218.4:c.4093G>T	ENSP00000480487.1:p.Gly1365Cys
ENST00000620121.4:c.4093G>T	ENSP00000481978.1:p.Gly1365Cys
NM_015338.5:c.4093G>T , LRG_630t1:c.4093G>T	NP_056153.2:p.Gly1365Cys
XM_006723727.2:c.4090G>T	XP_006723790.1:p.Gly1364Cys
XM_006723728.2:c.4063G>T	XP_006723791.1:p.Gly1355Cys
XM_006723730.2:c.4009G>T	XP_006723793.1:p.Gly1337Cys
XM_006723732.2:c.3910G>T	XP_006723795.1:p.Gly1304Cys
XM_006723733.1:c.3409G>T	XP_006723796.1:p.Gly1137Cys
XM_011528647.1:c.4357G>T	XP_011526949.1:p.Gly1453Cys
XM_011528648.1:c.4354G>T	XP_011526950.1:p.Gly1452Cys
XM_011528649.1:c.4273G>T	XP_011526951.1:p.Gly1425Cys
XM_011528650.1:c.4204G>T	XP_011526952.1:p.Gly1402Cys
XM_011528651.1:c.4072G>T	XP_011526953.1:p.Gly1358Cys
XM_011528652.1:c.4009G>T	XP_011526954.1:p.Gly1337Cys
NM_001363734.1:c.3910G>T	NP_001350663.1:p.Gly1304Cys
XM_006723727.3:c.4090G>T	XP_006723790.1:p.Gly1364Cys
XM_006723728.3:c.4063G>T	XP_006723791.1:p.Gly1355Cys
XM_006723730.4:c.4009G>T	XP_006723793.1:p.Gly1337Cys
XM_011528648.3:c.4354G>T	XP_011526950.1:p.Gly1452Cys
XM_011528652.2:c.4009G>T	XP_011526954.1:p.Gly1337Cys
XM_017027704.1:c.4009G>T	XP_016883193.1:p.Gly1337Cys
XM_017027705.1:c.4009G>T	XP_016883194.1:p.Gly1337Cys
XM_017027706.1:c.3940G>T	XP_016883195.1:p.Gly1314Cys
NM_015338.6:c.4093G>T MANE Select	NP_056153.2:p.Gly1365Cys