Canonical Allele Identifier: CA10652454

Gene: ASXL1

Linked Data

• dbSNP Id: rs745736272
• MyVariant Identifiers: chr20:g.31024429T>A (hg19) ; chr20:g.32436626T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436626T>A , CM000682.2:g.32436626T>A	GRCh38
NC_000020.10:g.31024429T>A , CM000682.1:g.31024429T>A	GRCh37
NC_000020.9:g.30488090T>A	NCBI36
NG_027868.1:g.83283T>A , LRG_630:g.83283T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3914T>A MANE Select	ENSP00000364839.4:p.Phe1305Tyr
ENST00000646985.1:c.3731T>A	ENSP00000495053.1:p.Phe1244Tyr
ENST00000647223.1:n.6267T>A
ENST00000651418.1:c.1870-1804T>A	ENSP00000499150.1:n.1870-1804T>A
ENST00000306058.9:c.3899T>A	ENSP00000305119.5:p.Phe1300Tyr
ENST00000375687.8:c.3914T>A	ENSP00000364839.4:p.Phe1305Tyr
ENST00000613218.4:c.3914T>A	ENSP00000480487.1:p.Phe1305Tyr
ENST00000620121.4:c.3914T>A	ENSP00000481978.1:p.Phe1305Tyr
NM_015338.5:c.3914T>A , LRG_630t1:c.3914T>A	NP_056153.2:p.Phe1305Tyr
XM_006723727.2:c.3911T>A	XP_006723790.1:p.Phe1304Tyr
XM_006723728.2:c.3884T>A	XP_006723791.1:p.Phe1295Tyr
XM_006723730.2:c.3830T>A	XP_006723793.1:p.Phe1277Tyr
XM_006723732.2:c.3731T>A	XP_006723795.1:p.Phe1244Tyr
XM_006723733.1:c.3230T>A	XP_006723796.1:p.Phe1077Tyr
XM_011528647.1:c.4178T>A	XP_011526949.1:p.Phe1393Tyr
XM_011528648.1:c.4175T>A	XP_011526950.1:p.Phe1392Tyr
XM_011528649.1:c.4094T>A	XP_011526951.1:p.Phe1365Tyr
XM_011528650.1:c.4025T>A	XP_011526952.1:p.Phe1342Tyr
XM_011528651.1:c.3893T>A	XP_011526953.1:p.Phe1298Tyr
XM_011528652.1:c.3830T>A	XP_011526954.1:p.Phe1277Tyr
NM_001363734.1:c.3731T>A	NP_001350663.1:p.Phe1244Tyr
XM_006723727.3:c.3911T>A	XP_006723790.1:p.Phe1304Tyr
XM_006723728.3:c.3884T>A	XP_006723791.1:p.Phe1295Tyr
XM_006723730.4:c.3830T>A	XP_006723793.1:p.Phe1277Tyr
XM_011528648.3:c.4175T>A	XP_011526950.1:p.Phe1392Tyr
XM_011528652.2:c.3830T>A	XP_011526954.1:p.Phe1277Tyr
XM_017027704.1:c.3830T>A	XP_016883193.1:p.Phe1277Tyr
XM_017027705.1:c.3830T>A	XP_016883194.1:p.Phe1277Tyr
XM_017027706.1:c.3761T>A	XP_016883195.1:p.Phe1254Tyr
NM_015338.6:c.3914T>A MANE Select	NP_056153.2:p.Phe1305Tyr