Canonical Allele Identifier: CA2360293442

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435883T= , CM000682.2:g.32435883T=	GRCh38
NC_000020.10:g.31023686T= , CM000682.1:g.31023686T=	GRCh37
NC_000020.9:g.30487347T=	NCBI36
NG_027868.1:g.82540T= , LRG_630:g.82540T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3171T= MANE Select	ENSP00000364839.4:p.Asp1057=
ENST00000646985.1:c.2988T=	ENSP00000495053.1:p.Asp996=
ENST00000647223.1:n.5524T=
ENST00000651418.1:c.1869+1302T=	ENSP00000499150.1:n.1869+1302T=
ENST00000306058.9:c.3156T=	ENSP00000305119.5:p.Asp1052=
ENST00000375687.8:c.3171T=	ENSP00000364839.4:p.Asp1057=
ENST00000613218.4:c.3171T=	ENSP00000480487.1:p.Asp1057=
ENST00000620121.4:c.3171T=	ENSP00000481978.1:p.Asp1057=
NM_015338.5:c.3171T= , LRG_630t1:c.3171T=	NP_056153.2:p.Asp1057=
XM_006723727.2:c.3168T=	XP_006723790.1:p.Asp1056=
XM_006723728.2:c.3141T=	XP_006723791.1:p.Asp1047=
XM_006723730.2:c.3087T=	XP_006723793.1:p.Asp1029=
XM_006723732.2:c.2988T=	XP_006723795.1:p.Asp996=
XM_006723733.1:c.2487T=	XP_006723796.1:p.Asp829=
XM_011528647.1:c.3435T=	XP_011526949.1:p.Asp1145=
XM_011528648.1:c.3432T=	XP_011526950.1:p.Asp1144=
XM_011528649.1:c.3351T=	XP_011526951.1:p.Asp1117=
XM_011528650.1:c.3282T=	XP_011526952.1:p.Asp1094=
XM_011528651.1:c.3150T=	XP_011526953.1:p.Asp1050=
XM_011528652.1:c.3087T=	XP_011526954.1:p.Asp1029=
NM_001363734.1:c.2988T=	NP_001350663.1:p.Asp996=
XM_006723727.3:c.3168T=	XP_006723790.1:p.Asp1056=
XM_006723728.3:c.3141T=	XP_006723791.1:p.Asp1047=
XM_006723730.4:c.3087T=	XP_006723793.1:p.Asp1029=
XM_011528648.3:c.3432T=	XP_011526950.1:p.Asp1144=
XM_011528652.2:c.3087T=	XP_011526954.1:p.Asp1029=
XM_017027704.1:c.3087T=	XP_016883193.1:p.Asp1029=
XM_017027705.1:c.3087T=	XP_016883194.1:p.Asp1029=
XM_017027706.1:c.3018T=	XP_016883195.1:p.Asp1006=
NM_015338.6:c.3171T= MANE Select	NP_056153.2:p.Asp1057=