Canonical Allele Identifier: CA510467243

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023947T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436144T>C , CM000682.2:g.32436144T>C	GRCh38
NC_000020.10:g.31023947T>C , CM000682.1:g.31023947T>C	GRCh37
NC_000020.9:g.30487608T>C	NCBI36
NG_027868.1:g.82801T>C , LRG_630:g.82801T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3432T>C MANE Select	ENSP00000364839.4:p.His1144=
ENST00000646985.1:c.3249T>C	ENSP00000495053.1:p.His1083=
ENST00000647223.1:n.5785T>C
ENST00000651418.1:c.1869+1563T>C	ENSP00000499150.1:n.1869+1563T>C
ENST00000306058.9:c.3417T>C	ENSP00000305119.5:p.His1139=
ENST00000375687.8:c.3432T>C	ENSP00000364839.4:p.His1144=
ENST00000613218.4:c.3432T>C	ENSP00000480487.1:p.His1144=
ENST00000620121.4:c.3432T>C	ENSP00000481978.1:p.His1144=
NM_015338.5:c.3432T>C , LRG_630t1:c.3432T>C	NP_056153.2:p.His1144=
XM_006723727.2:c.3429T>C	XP_006723790.1:p.His1143=
XM_006723728.2:c.3402T>C	XP_006723791.1:p.His1134=
XM_006723730.2:c.3348T>C	XP_006723793.1:p.His1116=
XM_006723732.2:c.3249T>C	XP_006723795.1:p.His1083=
XM_006723733.1:c.2748T>C	XP_006723796.1:p.His916=
XM_011528647.1:c.3696T>C	XP_011526949.1:p.His1232=
XM_011528648.1:c.3693T>C	XP_011526950.1:p.His1231=
XM_011528649.1:c.3612T>C	XP_011526951.1:p.His1204=
XM_011528650.1:c.3543T>C	XP_011526952.1:p.His1181=
XM_011528651.1:c.3411T>C	XP_011526953.1:p.His1137=
XM_011528652.1:c.3348T>C	XP_011526954.1:p.His1116=
NM_001363734.1:c.3249T>C	NP_001350663.1:p.His1083=
XM_006723727.3:c.3429T>C	XP_006723790.1:p.His1143=
XM_006723728.3:c.3402T>C	XP_006723791.1:p.His1134=
XM_006723730.4:c.3348T>C	XP_006723793.1:p.His1116=
XM_011528648.3:c.3693T>C	XP_011526950.1:p.His1231=
XM_011528652.2:c.3348T>C	XP_011526954.1:p.His1116=
XM_017027704.1:c.3348T>C	XP_016883193.1:p.His1116=
XM_017027705.1:c.3348T>C	XP_016883194.1:p.His1116=
XM_017027706.1:c.3279T>C	XP_016883195.1:p.His1093=
NM_015338.6:c.3432T>C MANE Select	NP_056153.2:p.His1144=