Canonical Allele Identifier: CA510467128

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023869A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436066A>C , CM000682.2:g.32436066A>C	GRCh38
NC_000020.10:g.31023869A>C , CM000682.1:g.31023869A>C	GRCh37
NC_000020.9:g.30487530A>C	NCBI36
NG_027868.1:g.82723A>C , LRG_630:g.82723A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3354A>C MANE Select	ENSP00000364839.4:p.Leu1118=
ENST00000646985.1:c.3171A>C	ENSP00000495053.1:p.Leu1057=
ENST00000647223.1:n.5707A>C
ENST00000651418.1:c.1869+1485A>C	ENSP00000499150.1:n.1869+1485A>C
ENST00000306058.9:c.3339A>C	ENSP00000305119.5:p.Leu1113=
ENST00000375687.8:c.3354A>C	ENSP00000364839.4:p.Leu1118=
ENST00000613218.4:c.3354A>C	ENSP00000480487.1:p.Leu1118=
ENST00000620121.4:c.3354A>C	ENSP00000481978.1:p.Leu1118=
NM_015338.5:c.3354A>C , LRG_630t1:c.3354A>C	NP_056153.2:p.Leu1118=
XM_006723727.2:c.3351A>C	XP_006723790.1:p.Leu1117=
XM_006723728.2:c.3324A>C	XP_006723791.1:p.Leu1108=
XM_006723730.2:c.3270A>C	XP_006723793.1:p.Leu1090=
XM_006723732.2:c.3171A>C	XP_006723795.1:p.Leu1057=
XM_006723733.1:c.2670A>C	XP_006723796.1:p.Leu890=
XM_011528647.1:c.3618A>C	XP_011526949.1:p.Leu1206=
XM_011528648.1:c.3615A>C	XP_011526950.1:p.Leu1205=
XM_011528649.1:c.3534A>C	XP_011526951.1:p.Leu1178=
XM_011528650.1:c.3465A>C	XP_011526952.1:p.Leu1155=
XM_011528651.1:c.3333A>C	XP_011526953.1:p.Leu1111=
XM_011528652.1:c.3270A>C	XP_011526954.1:p.Leu1090=
NM_001363734.1:c.3171A>C	NP_001350663.1:p.Leu1057=
XM_006723727.3:c.3351A>C	XP_006723790.1:p.Leu1117=
XM_006723728.3:c.3324A>C	XP_006723791.1:p.Leu1108=
XM_006723730.4:c.3270A>C	XP_006723793.1:p.Leu1090=
XM_011528648.3:c.3615A>C	XP_011526950.1:p.Leu1205=
XM_011528652.2:c.3270A>C	XP_011526954.1:p.Leu1090=
XM_017027704.1:c.3270A>C	XP_016883193.1:p.Leu1090=
XM_017027705.1:c.3270A>C	XP_016883194.1:p.Leu1090=
XM_017027706.1:c.3201A>C	XP_016883195.1:p.Leu1067=
NM_015338.6:c.3354A>C MANE Select	NP_056153.2:p.Leu1118=