Canonical Allele Identifier: CA408564306

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436748-T-C
• MyVariant Identifiers: chr20:g.31024551T>C (hg19) ; chr20:g.32436748T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436748T>C , CM000682.2:g.32436748T>C	GRCh38
NC_000020.10:g.31024551T>C , CM000682.1:g.31024551T>C	GRCh37
NC_000020.9:g.30488212T>C	NCBI36
NG_027868.1:g.83405T>C , LRG_630:g.83405T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4036T>C MANE Select	ENSP00000364839.4:p.Ser1346Pro
ENST00000646985.1:c.3853T>C	ENSP00000495053.1:p.Ser1285Pro
ENST00000647223.1:n.6389T>C
ENST00000651418.1:c.1870-1682T>C	ENSP00000499150.1:n.1870-1682T>C
ENST00000306058.9:c.4021T>C	ENSP00000305119.5:p.Ser1341Pro
ENST00000375687.8:c.4036T>C	ENSP00000364839.4:p.Ser1346Pro
ENST00000613218.4:c.4036T>C	ENSP00000480487.1:p.Ser1346Pro
ENST00000620121.4:c.4036T>C	ENSP00000481978.1:p.Ser1346Pro
NM_015338.5:c.4036T>C , LRG_630t1:c.4036T>C	NP_056153.2:p.Ser1346Pro
XM_006723727.2:c.4033T>C	XP_006723790.1:p.Ser1345Pro
XM_006723728.2:c.4006T>C	XP_006723791.1:p.Ser1336Pro
XM_006723730.2:c.3952T>C	XP_006723793.1:p.Ser1318Pro
XM_006723732.2:c.3853T>C	XP_006723795.1:p.Ser1285Pro
XM_006723733.1:c.3352T>C	XP_006723796.1:p.Ser1118Pro
XM_011528647.1:c.4300T>C	XP_011526949.1:p.Ser1434Pro
XM_011528648.1:c.4297T>C	XP_011526950.1:p.Ser1433Pro
XM_011528649.1:c.4216T>C	XP_011526951.1:p.Ser1406Pro
XM_011528650.1:c.4147T>C	XP_011526952.1:p.Ser1383Pro
XM_011528651.1:c.4015T>C	XP_011526953.1:p.Ser1339Pro
XM_011528652.1:c.3952T>C	XP_011526954.1:p.Ser1318Pro
NM_001363734.1:c.3853T>C	NP_001350663.1:p.Ser1285Pro
XM_006723727.3:c.4033T>C	XP_006723790.1:p.Ser1345Pro
XM_006723728.3:c.4006T>C	XP_006723791.1:p.Ser1336Pro
XM_006723730.4:c.3952T>C	XP_006723793.1:p.Ser1318Pro
XM_011528648.3:c.4297T>C	XP_011526950.1:p.Ser1433Pro
XM_011528652.2:c.3952T>C	XP_011526954.1:p.Ser1318Pro
XM_017027704.1:c.3952T>C	XP_016883193.1:p.Ser1318Pro
XM_017027705.1:c.3952T>C	XP_016883194.1:p.Ser1318Pro
XM_017027706.1:c.3883T>C	XP_016883195.1:p.Ser1295Pro
NM_015338.6:c.4036T>C MANE Select	NP_056153.2:p.Ser1346Pro