Canonical Allele Identifier: CA408564184

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024494G>T (hg19) ; chr20:g.32436691G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436691G>T , CM000682.2:g.32436691G>T	GRCh38
NC_000020.10:g.31024494G>T , CM000682.1:g.31024494G>T	GRCh37
NC_000020.9:g.30488155G>T	NCBI36
NG_027868.1:g.83348G>T , LRG_630:g.83348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3979G>T MANE Select	ENSP00000364839.4:p.Ala1327Ser
ENST00000646985.1:c.3796G>T	ENSP00000495053.1:p.Ala1266Ser
ENST00000647223.1:n.6332G>T
ENST00000651418.1:c.1870-1739G>T	ENSP00000499150.1:n.1870-1739G>T
ENST00000306058.9:c.3964G>T	ENSP00000305119.5:p.Ala1322Ser
ENST00000375687.8:c.3979G>T	ENSP00000364839.4:p.Ala1327Ser
ENST00000613218.4:c.3979G>T	ENSP00000480487.1:p.Ala1327Ser
ENST00000620121.4:c.3979G>T	ENSP00000481978.1:p.Ala1327Ser
NM_015338.5:c.3979G>T , LRG_630t1:c.3979G>T	NP_056153.2:p.Ala1327Ser
XM_006723727.2:c.3976G>T	XP_006723790.1:p.Ala1326Ser
XM_006723728.2:c.3949G>T	XP_006723791.1:p.Ala1317Ser
XM_006723730.2:c.3895G>T	XP_006723793.1:p.Ala1299Ser
XM_006723732.2:c.3796G>T	XP_006723795.1:p.Ala1266Ser
XM_006723733.1:c.3295G>T	XP_006723796.1:p.Ala1099Ser
XM_011528647.1:c.4243G>T	XP_011526949.1:p.Ala1415Ser
XM_011528648.1:c.4240G>T	XP_011526950.1:p.Ala1414Ser
XM_011528649.1:c.4159G>T	XP_011526951.1:p.Ala1387Ser
XM_011528650.1:c.4090G>T	XP_011526952.1:p.Ala1364Ser
XM_011528651.1:c.3958G>T	XP_011526953.1:p.Ala1320Ser
XM_011528652.1:c.3895G>T	XP_011526954.1:p.Ala1299Ser
NM_001363734.1:c.3796G>T	NP_001350663.1:p.Ala1266Ser
XM_006723727.3:c.3976G>T	XP_006723790.1:p.Ala1326Ser
XM_006723728.3:c.3949G>T	XP_006723791.1:p.Ala1317Ser
XM_006723730.4:c.3895G>T	XP_006723793.1:p.Ala1299Ser
XM_011528648.3:c.4240G>T	XP_011526950.1:p.Ala1414Ser
XM_011528652.2:c.3895G>T	XP_011526954.1:p.Ala1299Ser
XM_017027704.1:c.3895G>T	XP_016883193.1:p.Ala1299Ser
XM_017027705.1:c.3895G>T	XP_016883194.1:p.Ala1299Ser
XM_017027706.1:c.3826G>T	XP_016883195.1:p.Ala1276Ser
NM_015338.6:c.3979G>T MANE Select	NP_056153.2:p.Ala1327Ser