Canonical Allele Identifier: CA408563280

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024057G>C (hg19) ; chr20:g.32436254G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436254G>C , CM000682.2:g.32436254G>C	GRCh38
NC_000020.10:g.31024057G>C , CM000682.1:g.31024057G>C	GRCh37
NC_000020.9:g.30487718G>C	NCBI36
NG_027868.1:g.82911G>C , LRG_630:g.82911G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375687.10:c.3542G>C MANE Select	ENSP00000364839.4:p.Ser1181Thr
ENST00000646985.1:c.3359G>C	ENSP00000495053.1:p.Ser1120Thr
ENST00000647223.1:n.5895G>C
ENST00000651418.1:c.1869+1673G>C	ENSP00000499150.1:n.1869+1673G>C
ENST00000306058.9:c.3527G>C	ENSP00000305119.5:p.Ser1176Thr
ENST00000375687.8:c.3542G>C	ENSP00000364839.4:p.Ser1181Thr
ENST00000613218.4:c.3542G>C	ENSP00000480487.1:p.Ser1181Thr
ENST00000620121.4:c.3542G>C	ENSP00000481978.1:p.Ser1181Thr
NM_015338.5:c.3542G>C , LRG_630t1:c.3542G>C	NP_056153.2:p.Ser1181Thr
XM_006723727.2:c.3539G>C	XP_006723790.1:p.Ser1180Thr
XM_006723728.2:c.3512G>C	XP_006723791.1:p.Ser1171Thr
XM_006723730.2:c.3458G>C	XP_006723793.1:p.Ser1153Thr
XM_006723732.2:c.3359G>C	XP_006723795.1:p.Ser1120Thr
XM_006723733.1:c.2858G>C	XP_006723796.1:p.Ser953Thr
XM_011528647.1:c.3806G>C	XP_011526949.1:p.Ser1269Thr
XM_011528648.1:c.3803G>C	XP_011526950.1:p.Ser1268Thr
XM_011528649.1:c.3722G>C	XP_011526951.1:p.Ser1241Thr
XM_011528650.1:c.3653G>C	XP_011526952.1:p.Ser1218Thr
XM_011528651.1:c.3521G>C	XP_011526953.1:p.Ser1174Thr
XM_011528652.1:c.3458G>C	XP_011526954.1:p.Ser1153Thr
NM_001363734.1:c.3359G>C	NP_001350663.1:p.Ser1120Thr
XM_006723727.3:c.3539G>C	XP_006723790.1:p.Ser1180Thr
XM_006723728.3:c.3512G>C	XP_006723791.1:p.Ser1171Thr
XM_006723730.4:c.3458G>C	XP_006723793.1:p.Ser1153Thr
XM_011528648.3:c.3803G>C	XP_011526950.1:p.Ser1268Thr
XM_011528652.2:c.3458G>C	XP_011526954.1:p.Ser1153Thr
XM_017027704.1:c.3458G>C	XP_016883193.1:p.Ser1153Thr
XM_017027705.1:c.3458G>C	XP_016883194.1:p.Ser1153Thr
XM_017027706.1:c.3389G>C	XP_016883195.1:p.Ser1130Thr
NM_015338.6:c.3542G>C MANE Select	NP_056153.2:p.Ser1181Thr