Canonical Allele Identifier: CA510200436

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31015996T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428193T>G , CM000682.2:g.32428193T>G	GRCh38
NC_000020.10:g.31015996T>G , CM000682.1:g.31015996T>G	GRCh37
NC_000020.9:g.30479657T>G	NCBI36
NG_027868.1:g.74850T>G , LRG_630:g.74850T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.318T>G MANE Select	ENSP00000364839.4:p.Ala106=
ENST00000470145.3:n.261T>G
ENST00000643168.1:c.234T>G	ENSP00000495003.1:p.Ala78=
ENST00000644060.1:n.1122T>G
ENST00000644587.1:c.*157T>G	ENSP00000494813.1:n.*157T>G
ENST00000644615.1:n.22T>G
ENST00000645514.1:n.66T>G
ENST00000645688.1:c.234T>G	ENSP00000495488.1:p.Ala78=
ENST00000646985.1:c.288T>G	ENSP00000495053.1:p.Ala96=
ENST00000651418.1:c.318T>G	ENSP00000499150.1:p.Ala106=
ENST00000306058.9:c.303T>G	ENSP00000305119.5:p.Ala101=
ENST00000375687.8:c.318T>G	ENSP00000364839.4:p.Ala106=
ENST00000470145.2:n.261T>G
ENST00000613218.4:c.318T>G	ENSP00000480487.1:p.Ala106=
ENST00000620121.4:c.318T>G	ENSP00000481978.1:p.Ala106=
NM_015338.5:c.318T>G , LRG_630t1:c.318T>G	NP_056153.2:p.Ala106=
XM_006723727.2:c.315T>G	XP_006723790.1:p.Ala105=
XM_006723728.2:c.288T>G	XP_006723791.1:p.Ala96=
XM_006723730.2:c.234T>G	XP_006723793.1:p.Ala78=
XM_006723732.2:c.288T>G	XP_006723795.1:p.Ala96=
XM_011528647.1:c.582T>G	XP_011526949.1:p.Ala194=
XM_011528648.1:c.579T>G	XP_011526950.1:p.Ala193=
XM_011528649.1:c.498T>G	XP_011526951.1:p.Ala166=
XM_011528650.1:c.582T>G	XP_011526952.1:p.Ala194=
XM_011528651.1:c.297T>G	XP_011526953.1:p.Ala99=
XM_011528652.1:c.234T>G	XP_011526954.1:p.Ala78=
NM_001363734.1:c.288T>G	NP_001350663.1:p.Ala96=
XM_006723727.3:c.315T>G	XP_006723790.1:p.Ala105=
XM_006723728.3:c.288T>G	XP_006723791.1:p.Ala96=
XM_006723730.4:c.234T>G	XP_006723793.1:p.Ala78=
XM_011528648.3:c.579T>G	XP_011526950.1:p.Ala193=
XM_011528652.2:c.234T>G	XP_011526954.1:p.Ala78=
XM_017027704.1:c.234T>G	XP_016883193.1:p.Ala78=
XM_017027705.1:c.234T>G	XP_016883194.1:p.Ala78=
XM_017027706.1:c.318T>G	XP_016883195.1:p.Ala106=
NM_015338.6:c.318T>G MANE Select	NP_056153.2:p.Ala106=