Canonical Allele Identifier: CA9808536

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32434789C>T , CM000682.2:g.32434789C>T	GRCh38
NC_000020.10:g.31022592C>T , CM000682.1:g.31022592C>T	GRCh37
NC_000020.9:g.30486253C>T	NCBI36
NG_027868.1:g.81446C>T , LRG_630:g.81446C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.2077C>T MANE Select	ENSP00000364839.4:p.Arg693Ter
ENST00000646985.1:c.1894C>T	ENSP00000495053.1:p.Arg632Ter
ENST00000647223.1:n.4430C>T
ENST00000651418.1:c.1869+208C>T	ENSP00000499150.1:n.1869+208C>T
ENST00000306058.9:c.2062C>T	ENSP00000305119.5:p.Arg688Ter
ENST00000375687.8:c.2077C>T	ENSP00000364839.4:p.Arg693Ter
ENST00000613218.4:c.2077C>T	ENSP00000480487.1:p.Arg693Ter
ENST00000620121.4:c.2077C>T	ENSP00000481978.1:p.Arg693Ter
NM_015338.5:c.2077C>T , LRG_630t1:c.2077C>T	NP_056153.2:p.Arg693Ter
XM_006723727.2:c.2074C>T	XP_006723790.1:p.Arg692Ter
XM_006723728.2:c.2047C>T	XP_006723791.1:p.Arg683Ter
XM_006723730.2:c.1993C>T	XP_006723793.1:p.Arg665Ter
XM_006723732.2:c.1894C>T	XP_006723795.1:p.Arg632Ter
XM_006723733.1:c.1393C>T	XP_006723796.1:p.Arg465Ter
XM_011528647.1:c.2341C>T	XP_011526949.1:p.Arg781Ter
XM_011528648.1:c.2338C>T	XP_011526950.1:p.Arg780Ter
XM_011528649.1:c.2257C>T	XP_011526951.1:p.Arg753Ter
XM_011528650.1:c.2188C>T	XP_011526952.1:p.Arg730Ter
XM_011528651.1:c.2056C>T	XP_011526953.1:p.Arg686Ter
XM_011528652.1:c.1993C>T	XP_011526954.1:p.Arg665Ter
NM_001363734.1:c.1894C>T	NP_001350663.1:p.Arg632Ter
XM_006723727.3:c.2074C>T	XP_006723790.1:p.Arg692Ter
XM_006723728.3:c.2047C>T	XP_006723791.1:p.Arg683Ter
XM_006723730.4:c.1993C>T	XP_006723793.1:p.Arg665Ter
XM_011528648.3:c.2338C>T	XP_011526950.1:p.Arg780Ter
XM_011528652.2:c.1993C>T	XP_011526954.1:p.Arg665Ter
XM_017027704.1:c.1993C>T	XP_016883193.1:p.Arg665Ter
XM_017027705.1:c.1993C>T	XP_016883194.1:p.Arg665Ter
XM_017027706.1:c.1924C>T	XP_016883195.1:p.Arg642Ter
NM_015338.6:c.2077C>T MANE Select	NP_056153.2:p.Arg693Ter