Canonical Allele Identifier: CA510467240
Gene: ASXL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.31023938C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436135C>T , CM000682.2:g.32436135C>T GRCh38
NC_000020.10:g.31023938C>T , CM000682.1:g.31023938C>T GRCh37
NC_000020.9:g.30487599C>T NCBI36
NG_027868.1:g.82792C>T , LRG_630:g.82792C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3423C>T MANE Select ENSP00000364839.4:p.Asp1141=
ENST00000646985.1:c.3240C>T ENSP00000495053.1:p.Asp1080=
ENST00000647223.1:n.5776C>T
ENST00000651418.1:c.1869+1554C>T ENSP00000499150.1:n.1869+1554C>T
ENST00000306058.9:c.3408C>T ENSP00000305119.5:p.Asp1136=
ENST00000375687.8:c.3423C>T ENSP00000364839.4:p.Asp1141=
ENST00000613218.4:c.3423C>T ENSP00000480487.1:p.Asp1141=
ENST00000620121.4:c.3423C>T ENSP00000481978.1:p.Asp1141=
NM_015338.5:c.3423C>T , LRG_630t1:c.3423C>T NP_056153.2:p.Asp1141=
XM_006723727.2:c.3420C>T XP_006723790.1:p.Asp1140=
XM_006723728.2:c.3393C>T XP_006723791.1:p.Asp1131=
XM_006723730.2:c.3339C>T XP_006723793.1:p.Asp1113=
XM_006723732.2:c.3240C>T XP_006723795.1:p.Asp1080=
XM_006723733.1:c.2739C>T XP_006723796.1:p.Asp913=
XM_011528647.1:c.3687C>T XP_011526949.1:p.Asp1229=
XM_011528648.1:c.3684C>T XP_011526950.1:p.Asp1228=
XM_011528649.1:c.3603C>T XP_011526951.1:p.Asp1201=
XM_011528650.1:c.3534C>T XP_011526952.1:p.Asp1178=
XM_011528651.1:c.3402C>T XP_011526953.1:p.Asp1134=
XM_011528652.1:c.3339C>T XP_011526954.1:p.Asp1113=
NM_001363734.1:c.3240C>T NP_001350663.1:p.Asp1080=
XM_006723727.3:c.3420C>T XP_006723790.1:p.Asp1140=
XM_006723728.3:c.3393C>T XP_006723791.1:p.Asp1131=
XM_006723730.4:c.3339C>T XP_006723793.1:p.Asp1113=
XM_011528648.3:c.3684C>T XP_011526950.1:p.Asp1228=
XM_011528652.2:c.3339C>T XP_011526954.1:p.Asp1113=
XM_017027704.1:c.3339C>T XP_016883193.1:p.Asp1113=
XM_017027705.1:c.3339C>T XP_016883194.1:p.Asp1113=
XM_017027706.1:c.3270C>T XP_016883195.1:p.Asp1090=
NM_015338.6:c.3423C>T MANE Select NP_056153.2:p.Asp1141=