Canonical Allele Identifier: CA510467376

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024157T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436354T>C , CM000682.2:g.32436354T>C	GRCh38
NC_000020.10:g.31024157T>C , CM000682.1:g.31024157T>C	GRCh37
NC_000020.9:g.30487818T>C	NCBI36
NG_027868.1:g.83011T>C , LRG_630:g.83011T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375687.10:c.3642T>C MANE Select	ENSP00000364839.4:p.His1214=
ENST00000646985.1:c.3459T>C	ENSP00000495053.1:p.His1153=
ENST00000647223.1:n.5995T>C
ENST00000651418.1:c.1869+1773T>C	ENSP00000499150.1:n.1869+1773T>C
ENST00000306058.9:c.3627T>C	ENSP00000305119.5:p.His1209=
ENST00000375687.8:c.3642T>C	ENSP00000364839.4:p.His1214=
ENST00000613218.4:c.3642T>C	ENSP00000480487.1:p.His1214=
ENST00000620121.4:c.3642T>C	ENSP00000481978.1:p.His1214=
NM_015338.5:c.3642T>C , LRG_630t1:c.3642T>C	NP_056153.2:p.His1214=
XM_006723727.2:c.3639T>C	XP_006723790.1:p.His1213=
XM_006723728.2:c.3612T>C	XP_006723791.1:p.His1204=
XM_006723730.2:c.3558T>C	XP_006723793.1:p.His1186=
XM_006723732.2:c.3459T>C	XP_006723795.1:p.His1153=
XM_006723733.1:c.2958T>C	XP_006723796.1:p.His986=
XM_011528647.1:c.3906T>C	XP_011526949.1:p.His1302=
XM_011528648.1:c.3903T>C	XP_011526950.1:p.His1301=
XM_011528649.1:c.3822T>C	XP_011526951.1:p.His1274=
XM_011528650.1:c.3753T>C	XP_011526952.1:p.His1251=
XM_011528651.1:c.3621T>C	XP_011526953.1:p.His1207=
XM_011528652.1:c.3558T>C	XP_011526954.1:p.His1186=
NM_001363734.1:c.3459T>C	NP_001350663.1:p.His1153=
XM_006723727.3:c.3639T>C	XP_006723790.1:p.His1213=
XM_006723728.3:c.3612T>C	XP_006723791.1:p.His1204=
XM_006723730.4:c.3558T>C	XP_006723793.1:p.His1186=
XM_011528648.3:c.3903T>C	XP_011526950.1:p.His1301=
XM_011528652.2:c.3558T>C	XP_011526954.1:p.His1186=
XM_017027704.1:c.3558T>C	XP_016883193.1:p.His1186=
XM_017027705.1:c.3558T>C	XP_016883194.1:p.His1186=
XM_017027706.1:c.3489T>C	XP_016883195.1:p.His1163=
NM_015338.6:c.3642T>C MANE Select	NP_056153.2:p.His1214=