Canonical Allele Identifier: CA510467294

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024061T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436258T>C , CM000682.2:g.32436258T>C	GRCh38
NC_000020.10:g.31024061T>C , CM000682.1:g.31024061T>C	GRCh37
NC_000020.9:g.30487722T>C	NCBI36
NG_027868.1:g.82915T>C , LRG_630:g.82915T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375687.10:c.3546T>C MANE Select	ENSP00000364839.4:p.Cys1182=
ENST00000646985.1:c.3363T>C	ENSP00000495053.1:p.Cys1121=
ENST00000647223.1:n.5899T>C
ENST00000651418.1:c.1869+1677T>C	ENSP00000499150.1:n.1869+1677T>C
ENST00000306058.9:c.3531T>C	ENSP00000305119.5:p.Cys1177=
ENST00000375687.8:c.3546T>C	ENSP00000364839.4:p.Cys1182=
ENST00000613218.4:c.3546T>C	ENSP00000480487.1:p.Cys1182=
ENST00000620121.4:c.3546T>C	ENSP00000481978.1:p.Cys1182=
NM_015338.5:c.3546T>C , LRG_630t1:c.3546T>C	NP_056153.2:p.Cys1182=
XM_006723727.2:c.3543T>C	XP_006723790.1:p.Cys1181=
XM_006723728.2:c.3516T>C	XP_006723791.1:p.Cys1172=
XM_006723730.2:c.3462T>C	XP_006723793.1:p.Cys1154=
XM_006723732.2:c.3363T>C	XP_006723795.1:p.Cys1121=
XM_006723733.1:c.2862T>C	XP_006723796.1:p.Cys954=
XM_011528647.1:c.3810T>C	XP_011526949.1:p.Cys1270=
XM_011528648.1:c.3807T>C	XP_011526950.1:p.Cys1269=
XM_011528649.1:c.3726T>C	XP_011526951.1:p.Cys1242=
XM_011528650.1:c.3657T>C	XP_011526952.1:p.Cys1219=
XM_011528651.1:c.3525T>C	XP_011526953.1:p.Cys1175=
XM_011528652.1:c.3462T>C	XP_011526954.1:p.Cys1154=
NM_001363734.1:c.3363T>C	NP_001350663.1:p.Cys1121=
XM_006723727.3:c.3543T>C	XP_006723790.1:p.Cys1181=
XM_006723728.3:c.3516T>C	XP_006723791.1:p.Cys1172=
XM_006723730.4:c.3462T>C	XP_006723793.1:p.Cys1154=
XM_011528648.3:c.3807T>C	XP_011526950.1:p.Cys1269=
XM_011528652.2:c.3462T>C	XP_011526954.1:p.Cys1154=
XM_017027704.1:c.3462T>C	XP_016883193.1:p.Cys1154=
XM_017027705.1:c.3462T>C	XP_016883194.1:p.Cys1154=
XM_017027706.1:c.3393T>C	XP_016883195.1:p.Cys1131=
NM_015338.6:c.3546T>C MANE Select	NP_056153.2:p.Cys1182=