Canonical Allele Identifier: CA408563961

Gene: ASXL1

Linked Data

• dbSNP Id: rs2145388752
• MyVariant Identifiers: chr20:g.31024383G>C (hg19) ; chr20:g.32436580G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436580G>C , CM000682.2:g.32436580G>C	GRCh38
NC_000020.10:g.31024383G>C , CM000682.1:g.31024383G>C	GRCh37
NC_000020.9:g.30488044G>C	NCBI36
NG_027868.1:g.83237G>C , LRG_630:g.83237G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3868G>C MANE Select	ENSP00000364839.4:p.Ala1290Pro
ENST00000646985.1:c.3685G>C	ENSP00000495053.1:p.Ala1229Pro
ENST00000647223.1:n.6221G>C
ENST00000651418.1:c.1870-1850G>C	ENSP00000499150.1:n.1870-1850G>C
ENST00000306058.9:c.3853G>C	ENSP00000305119.5:p.Ala1285Pro
ENST00000375687.8:c.3868G>C	ENSP00000364839.4:p.Ala1290Pro
ENST00000613218.4:c.3868G>C	ENSP00000480487.1:p.Ala1290Pro
ENST00000620121.4:c.3868G>C	ENSP00000481978.1:p.Ala1290Pro
NM_015338.5:c.3868G>C , LRG_630t1:c.3868G>C	NP_056153.2:p.Ala1290Pro
XM_006723727.2:c.3865G>C	XP_006723790.1:p.Ala1289Pro
XM_006723728.2:c.3838G>C	XP_006723791.1:p.Ala1280Pro
XM_006723730.2:c.3784G>C	XP_006723793.1:p.Ala1262Pro
XM_006723732.2:c.3685G>C	XP_006723795.1:p.Ala1229Pro
XM_006723733.1:c.3184G>C	XP_006723796.1:p.Ala1062Pro
XM_011528647.1:c.4132G>C	XP_011526949.1:p.Ala1378Pro
XM_011528648.1:c.4129G>C	XP_011526950.1:p.Ala1377Pro
XM_011528649.1:c.4048G>C	XP_011526951.1:p.Ala1350Pro
XM_011528650.1:c.3979G>C	XP_011526952.1:p.Ala1327Pro
XM_011528651.1:c.3847G>C	XP_011526953.1:p.Ala1283Pro
XM_011528652.1:c.3784G>C	XP_011526954.1:p.Ala1262Pro
NM_001363734.1:c.3685G>C	NP_001350663.1:p.Ala1229Pro
XM_006723727.3:c.3865G>C	XP_006723790.1:p.Ala1289Pro
XM_006723728.3:c.3838G>C	XP_006723791.1:p.Ala1280Pro
XM_006723730.4:c.3784G>C	XP_006723793.1:p.Ala1262Pro
XM_011528648.3:c.4129G>C	XP_011526950.1:p.Ala1377Pro
XM_011528652.2:c.3784G>C	XP_011526954.1:p.Ala1262Pro
XM_017027704.1:c.3784G>C	XP_016883193.1:p.Ala1262Pro
XM_017027705.1:c.3784G>C	XP_016883194.1:p.Ala1262Pro
XM_017027706.1:c.3715G>C	XP_016883195.1:p.Ala1239Pro
NM_015338.6:c.3868G>C MANE Select	NP_056153.2:p.Ala1290Pro