Canonical Allele Identifier: CA408562637

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023751C>T (hg19) ; chr20:g.32435948C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435948C>T , CM000682.2:g.32435948C>T	GRCh38
NC_000020.10:g.31023751C>T , CM000682.1:g.31023751C>T	GRCh37
NC_000020.9:g.30487412C>T	NCBI36
NG_027868.1:g.82605C>T , LRG_630:g.82605C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3236C>T MANE Select	ENSP00000364839.4:p.Ser1079Phe
ENST00000646985.1:c.3053C>T	ENSP00000495053.1:p.Ser1018Phe
ENST00000647223.1:n.5589C>T
ENST00000651418.1:c.1869+1367C>T	ENSP00000499150.1:n.1869+1367C>T
ENST00000306058.9:c.3221C>T	ENSP00000305119.5:p.Ser1074Phe
ENST00000375687.8:c.3236C>T	ENSP00000364839.4:p.Ser1079Phe
ENST00000613218.4:c.3236C>T	ENSP00000480487.1:p.Ser1079Phe
ENST00000620121.4:c.3236C>T	ENSP00000481978.1:p.Ser1079Phe
NM_015338.5:c.3236C>T , LRG_630t1:c.3236C>T	NP_056153.2:p.Ser1079Phe
XM_006723727.2:c.3233C>T	XP_006723790.1:p.Ser1078Phe
XM_006723728.2:c.3206C>T	XP_006723791.1:p.Ser1069Phe
XM_006723730.2:c.3152C>T	XP_006723793.1:p.Ser1051Phe
XM_006723732.2:c.3053C>T	XP_006723795.1:p.Ser1018Phe
XM_006723733.1:c.2552C>T	XP_006723796.1:p.Ser851Phe
XM_011528647.1:c.3500C>T	XP_011526949.1:p.Ser1167Phe
XM_011528648.1:c.3497C>T	XP_011526950.1:p.Ser1166Phe
XM_011528649.1:c.3416C>T	XP_011526951.1:p.Ser1139Phe
XM_011528650.1:c.3347C>T	XP_011526952.1:p.Ser1116Phe
XM_011528651.1:c.3215C>T	XP_011526953.1:p.Ser1072Phe
XM_011528652.1:c.3152C>T	XP_011526954.1:p.Ser1051Phe
NM_001363734.1:c.3053C>T	NP_001350663.1:p.Ser1018Phe
XM_006723727.3:c.3233C>T	XP_006723790.1:p.Ser1078Phe
XM_006723728.3:c.3206C>T	XP_006723791.1:p.Ser1069Phe
XM_006723730.4:c.3152C>T	XP_006723793.1:p.Ser1051Phe
XM_011528648.3:c.3497C>T	XP_011526950.1:p.Ser1166Phe
XM_011528652.2:c.3152C>T	XP_011526954.1:p.Ser1051Phe
XM_017027704.1:c.3152C>T	XP_016883193.1:p.Ser1051Phe
XM_017027705.1:c.3152C>T	XP_016883194.1:p.Ser1051Phe
XM_017027706.1:c.3083C>T	XP_016883195.1:p.Ser1028Phe
NM_015338.6:c.3236C>T MANE Select	NP_056153.2:p.Ser1079Phe