Canonical Allele Identifier: CA408563945

Gene: ASXL1

Linked Data

• dbSNP Id: rs2011901981
• MyVariant Identifiers: chr20:g.31024373G>C (hg19) ; chr20:g.32436570G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436570G>C , CM000682.2:g.32436570G>C	GRCh38
NC_000020.10:g.31024373G>C , CM000682.1:g.31024373G>C	GRCh37
NC_000020.9:g.30488034G>C	NCBI36
NG_027868.1:g.83227G>C , LRG_630:g.83227G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3858G>C MANE Select	ENSP00000364839.4:p.Gln1286His
ENST00000646985.1:c.3675G>C	ENSP00000495053.1:p.Gln1225His
ENST00000647223.1:n.6211G>C
ENST00000651418.1:c.1870-1860G>C	ENSP00000499150.1:n.1870-1860G>C
ENST00000306058.9:c.3843G>C	ENSP00000305119.5:p.Gln1281His
ENST00000375687.8:c.3858G>C	ENSP00000364839.4:p.Gln1286His
ENST00000613218.4:c.3858G>C	ENSP00000480487.1:p.Gln1286His
ENST00000620121.4:c.3858G>C	ENSP00000481978.1:p.Gln1286His
NM_015338.5:c.3858G>C , LRG_630t1:c.3858G>C	NP_056153.2:p.Gln1286His
XM_006723727.2:c.3855G>C	XP_006723790.1:p.Gln1285His
XM_006723728.2:c.3828G>C	XP_006723791.1:p.Gln1276His
XM_006723730.2:c.3774G>C	XP_006723793.1:p.Gln1258His
XM_006723732.2:c.3675G>C	XP_006723795.1:p.Gln1225His
XM_006723733.1:c.3174G>C	XP_006723796.1:p.Gln1058His
XM_011528647.1:c.4122G>C	XP_011526949.1:p.Gln1374His
XM_011528648.1:c.4119G>C	XP_011526950.1:p.Gln1373His
XM_011528649.1:c.4038G>C	XP_011526951.1:p.Gln1346His
XM_011528650.1:c.3969G>C	XP_011526952.1:p.Gln1323His
XM_011528651.1:c.3837G>C	XP_011526953.1:p.Gln1279His
XM_011528652.1:c.3774G>C	XP_011526954.1:p.Gln1258His
NM_001363734.1:c.3675G>C	NP_001350663.1:p.Gln1225His
XM_006723727.3:c.3855G>C	XP_006723790.1:p.Gln1285His
XM_006723728.3:c.3828G>C	XP_006723791.1:p.Gln1276His
XM_006723730.4:c.3774G>C	XP_006723793.1:p.Gln1258His
XM_011528648.3:c.4119G>C	XP_011526950.1:p.Gln1373His
XM_011528652.2:c.3774G>C	XP_011526954.1:p.Gln1258His
XM_017027704.1:c.3774G>C	XP_016883193.1:p.Gln1258His
XM_017027705.1:c.3774G>C	XP_016883194.1:p.Gln1258His
XM_017027706.1:c.3705G>C	XP_016883195.1:p.Gln1235His
NM_015338.6:c.3858G>C MANE Select	NP_056153.2:p.Gln1286His