Canonical Allele Identifier: CA408562528

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023699C>A (hg19) ; chr20:g.32435896C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435896C>A , CM000682.2:g.32435896C>A	GRCh38
NC_000020.10:g.31023699C>A , CM000682.1:g.31023699C>A	GRCh37
NC_000020.9:g.30487360C>A	NCBI36
NG_027868.1:g.82553C>A , LRG_630:g.82553C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3184C>A MANE Select	ENSP00000364839.4:p.Pro1062Thr
ENST00000646985.1:c.3001C>A	ENSP00000495053.1:p.Pro1001Thr
ENST00000647223.1:n.5537C>A
ENST00000651418.1:c.1869+1315C>A	ENSP00000499150.1:n.1869+1315C>A
ENST00000306058.9:c.3169C>A	ENSP00000305119.5:p.Pro1057Thr
ENST00000375687.8:c.3184C>A	ENSP00000364839.4:p.Pro1062Thr
ENST00000613218.4:c.3184C>A	ENSP00000480487.1:p.Pro1062Thr
ENST00000620121.4:c.3184C>A	ENSP00000481978.1:p.Pro1062Thr
NM_015338.5:c.3184C>A , LRG_630t1:c.3184C>A	NP_056153.2:p.Pro1062Thr
XM_006723727.2:c.3181C>A	XP_006723790.1:p.Pro1061Thr
XM_006723728.2:c.3154C>A	XP_006723791.1:p.Pro1052Thr
XM_006723730.2:c.3100C>A	XP_006723793.1:p.Pro1034Thr
XM_006723732.2:c.3001C>A	XP_006723795.1:p.Pro1001Thr
XM_006723733.1:c.2500C>A	XP_006723796.1:p.Pro834Thr
XM_011528647.1:c.3448C>A	XP_011526949.1:p.Pro1150Thr
XM_011528648.1:c.3445C>A	XP_011526950.1:p.Pro1149Thr
XM_011528649.1:c.3364C>A	XP_011526951.1:p.Pro1122Thr
XM_011528650.1:c.3295C>A	XP_011526952.1:p.Pro1099Thr
XM_011528651.1:c.3163C>A	XP_011526953.1:p.Pro1055Thr
XM_011528652.1:c.3100C>A	XP_011526954.1:p.Pro1034Thr
NM_001363734.1:c.3001C>A	NP_001350663.1:p.Pro1001Thr
XM_006723727.3:c.3181C>A	XP_006723790.1:p.Pro1061Thr
XM_006723728.3:c.3154C>A	XP_006723791.1:p.Pro1052Thr
XM_006723730.4:c.3100C>A	XP_006723793.1:p.Pro1034Thr
XM_011528648.3:c.3445C>A	XP_011526950.1:p.Pro1149Thr
XM_011528652.2:c.3100C>A	XP_011526954.1:p.Pro1034Thr
XM_017027704.1:c.3100C>A	XP_016883193.1:p.Pro1034Thr
XM_017027705.1:c.3100C>A	XP_016883194.1:p.Pro1034Thr
XM_017027706.1:c.3031C>A	XP_016883195.1:p.Pro1011Thr
NM_015338.6:c.3184C>A MANE Select	NP_056153.2:p.Pro1062Thr