Canonical Allele Identifier: CA2360293654
Gene: ASXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436344_32436348delinsACTCC , CM000682.2:g.32436344_32436348delinsACTCC GRCh38
NC_000020.10:g.31024147_31024151delinsACTCC , CM000682.1:g.31024147_31024151delinsACTCC GRCh37
NC_000020.9:g.30487808_30487812delinsACTCC NCBI36
NG_027868.1:g.83001_83005delinsACTCC , LRG_630:g.83001_83005delinsACTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000375687.10:c.3632_3636delinsACTCC MANE Select ENSP00000364839.4:p.Asp1211=
ENST00000646985.1:c.3449_3453delinsACTCC ENSP00000495053.1:p.Asp1150=
ENST00000647223.1:n.5985_5989delinsACTCC
ENST00000651418.1:c.1869+1763_1869+1767delinsACTCC ENSP00000499150.1:n.1869+1763_1869+1767de...
ENST00000306058.9:c.3617_3621delinsACTCC ENSP00000305119.5:p.Asp1206=
ENST00000375687.8:c.3632_3636delinsACTCC ENSP00000364839.4:p.Asp1211=
ENST00000613218.4:c.3632_3636delinsACTCC ENSP00000480487.1:p.Asp1211=
ENST00000620121.4:c.3632_3636delinsACTCC ENSP00000481978.1:p.Asp1211=
NM_015338.5:c.3632_3636delinsACTCC , LRG_630t1:c.3632_3636delinsACTCC NP_056153.2:p.Asp1211=
XM_006723727.2:c.3629_3633delinsACTCC XP_006723790.1:p.Asp1210=
XM_006723728.2:c.3602_3606delinsACTCC XP_006723791.1:p.Asp1201=
XM_006723730.2:c.3548_3552delinsACTCC XP_006723793.1:p.Asp1183=
XM_006723732.2:c.3449_3453delinsACTCC XP_006723795.1:p.Asp1150=
XM_006723733.1:c.2948_2952delinsACTCC XP_006723796.1:p.Asp983=
XM_011528647.1:c.3896_3900delinsACTCC XP_011526949.1:p.Asp1299=
XM_011528648.1:c.3893_3897delinsACTCC XP_011526950.1:p.Asp1298=
XM_011528649.1:c.3812_3816delinsACTCC XP_011526951.1:p.Asp1271=
XM_011528650.1:c.3743_3747delinsACTCC XP_011526952.1:p.Asp1248=
XM_011528651.1:c.3611_3615delinsACTCC XP_011526953.1:p.Asp1204=
XM_011528652.1:c.3548_3552delinsACTCC XP_011526954.1:p.Asp1183=
NM_001363734.1:c.3449_3453delinsACTCC NP_001350663.1:p.Asp1150=
XM_006723727.3:c.3629_3633delinsACTCC XP_006723790.1:p.Asp1210=
XM_006723728.3:c.3602_3606delinsACTCC XP_006723791.1:p.Asp1201=
XM_006723730.4:c.3548_3552delinsACTCC XP_006723793.1:p.Asp1183=
XM_011528648.3:c.3893_3897delinsACTCC XP_011526950.1:p.Asp1298=
XM_011528652.2:c.3548_3552delinsACTCC XP_011526954.1:p.Asp1183=
XM_017027704.1:c.3548_3552delinsACTCC XP_016883193.1:p.Asp1183=
XM_017027705.1:c.3548_3552delinsACTCC XP_016883194.1:p.Asp1183=
XM_017027706.1:c.3479_3483delinsACTCC XP_016883195.1:p.Asp1160=
NM_015338.6:c.3632_3636delinsACTCC MANE Select NP_056153.2:p.Asp1211=