Canonical Allele Identifier: CA408551567

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31016010G>C (hg19) ; chr20:g.32428207G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428207G>C , CM000682.2:g.32428207G>C	GRCh38
NC_000020.10:g.31016010G>C , CM000682.1:g.31016010G>C	GRCh37
NC_000020.9:g.30479671G>C	NCBI36
NG_027868.1:g.74864G>C , LRG_630:g.74864G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.332G>C MANE Select	ENSP00000364839.4:p.Cys111Ser
ENST00000470145.3:n.275G>C
ENST00000643168.1:c.248G>C	ENSP00000495003.1:p.Cys83Ser
ENST00000644060.1:n.1136G>C
ENST00000644587.1:c.*171G>C	ENSP00000494813.1:n.*171G>C
ENST00000644615.1:n.36G>C
ENST00000645514.1:n.80G>C
ENST00000646985.1:c.302G>C	ENSP00000495053.1:p.Cys101Ser
ENST00000651418.1:c.332G>C	ENSP00000499150.1:p.Cys111Ser
ENST00000306058.9:c.317G>C	ENSP00000305119.5:p.Cys106Ser
ENST00000375687.8:c.332G>C	ENSP00000364839.4:p.Cys111Ser
ENST00000470145.2:n.275G>C
ENST00000613218.4:c.332G>C	ENSP00000480487.1:p.Cys111Ser
ENST00000620121.4:c.332G>C	ENSP00000481978.1:p.Cys111Ser
NM_015338.5:c.332G>C , LRG_630t1:c.332G>C	NP_056153.2:p.Cys111Ser
XM_006723727.2:c.329G>C	XP_006723790.1:p.Cys110Ser
XM_006723728.2:c.302G>C	XP_006723791.1:p.Cys101Ser
XM_006723730.2:c.248G>C	XP_006723793.1:p.Cys83Ser
XM_006723732.2:c.302G>C	XP_006723795.1:p.Cys101Ser
XM_011528647.1:c.596G>C	XP_011526949.1:p.Cys199Ser
XM_011528648.1:c.593G>C	XP_011526950.1:p.Cys198Ser
XM_011528649.1:c.512G>C	XP_011526951.1:p.Cys171Ser
XM_011528650.1:c.596G>C	XP_011526952.1:p.Cys199Ser
XM_011528651.1:c.311G>C	XP_011526953.1:p.Cys104Ser
XM_011528652.1:c.248G>C	XP_011526954.1:p.Cys83Ser
NM_001363734.1:c.302G>C	NP_001350663.1:p.Cys101Ser
XM_006723727.3:c.329G>C	XP_006723790.1:p.Cys110Ser
XM_006723728.3:c.302G>C	XP_006723791.1:p.Cys101Ser
XM_006723730.4:c.248G>C	XP_006723793.1:p.Cys83Ser
XM_011528648.3:c.593G>C	XP_011526950.1:p.Cys198Ser
XM_011528652.2:c.248G>C	XP_011526954.1:p.Cys83Ser
XM_017027704.1:c.248G>C	XP_016883193.1:p.Cys83Ser
XM_017027705.1:c.248G>C	XP_016883194.1:p.Cys83Ser
XM_017027706.1:c.332G>C	XP_016883195.1:p.Cys111Ser
NM_015338.6:c.332G>C MANE Select	NP_056153.2:p.Cys111Ser