Canonical Allele Identifier: CA408564466

Gene: ASXL1

Linked Data

• dbSNP Id: rs2145392261
• MyVariant Identifiers: chr20:g.31024625G>C (hg19) ; chr20:g.32436822G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436822G>C , CM000682.2:g.32436822G>C	GRCh38
NC_000020.10:g.31024625G>C , CM000682.1:g.31024625G>C	GRCh37
NC_000020.9:g.30488286G>C	NCBI36
NG_027868.1:g.83479G>C , LRG_630:g.83479G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4110G>C MANE Select	ENSP00000364839.4:p.Glu1370Asp
ENST00000646985.1:c.3927G>C	ENSP00000495053.1:p.Glu1309Asp
ENST00000647223.1:n.6463G>C
ENST00000651418.1:c.1870-1608G>C	ENSP00000499150.1:n.1870-1608G>C
ENST00000306058.9:c.4095G>C	ENSP00000305119.5:p.Glu1365Asp
ENST00000375687.8:c.4110G>C	ENSP00000364839.4:p.Glu1370Asp
ENST00000613218.4:c.4110G>C	ENSP00000480487.1:p.Glu1370Asp
ENST00000620121.4:c.4110G>C	ENSP00000481978.1:p.Glu1370Asp
NM_015338.5:c.4110G>C , LRG_630t1:c.4110G>C	NP_056153.2:p.Glu1370Asp
XM_006723727.2:c.4107G>C	XP_006723790.1:p.Glu1369Asp
XM_006723728.2:c.4080G>C	XP_006723791.1:p.Glu1360Asp
XM_006723730.2:c.4026G>C	XP_006723793.1:p.Glu1342Asp
XM_006723732.2:c.3927G>C	XP_006723795.1:p.Glu1309Asp
XM_006723733.1:c.3426G>C	XP_006723796.1:p.Glu1142Asp
XM_011528647.1:c.4374G>C	XP_011526949.1:p.Glu1458Asp
XM_011528648.1:c.4371G>C	XP_011526950.1:p.Glu1457Asp
XM_011528649.1:c.4290G>C	XP_011526951.1:p.Glu1430Asp
XM_011528650.1:c.4221G>C	XP_011526952.1:p.Glu1407Asp
XM_011528651.1:c.4089G>C	XP_011526953.1:p.Glu1363Asp
XM_011528652.1:c.4026G>C	XP_011526954.1:p.Glu1342Asp
NM_001363734.1:c.3927G>C	NP_001350663.1:p.Glu1309Asp
XM_006723727.3:c.4107G>C	XP_006723790.1:p.Glu1369Asp
XM_006723728.3:c.4080G>C	XP_006723791.1:p.Glu1360Asp
XM_006723730.4:c.4026G>C	XP_006723793.1:p.Glu1342Asp
XM_011528648.3:c.4371G>C	XP_011526950.1:p.Glu1457Asp
XM_011528652.2:c.4026G>C	XP_011526954.1:p.Glu1342Asp
XM_017027704.1:c.4026G>C	XP_016883193.1:p.Glu1342Asp
XM_017027705.1:c.4026G>C	XP_016883194.1:p.Glu1342Asp
XM_017027706.1:c.3957G>C	XP_016883195.1:p.Glu1319Asp
NM_015338.6:c.4110G>C MANE Select	NP_056153.2:p.Glu1370Asp