Canonical Allele Identifier: CA408563412
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436319A>G , CM000682.2:g.32436319A>G GRCh38
NC_000020.10:g.31024122A>G , CM000682.1:g.31024122A>G GRCh37
NC_000020.9:g.30487783A>G NCBI36
NG_027868.1:g.82976A>G , LRG_630:g.82976A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3607A>G MANE Select ENSP00000364839.4:p.Asn1203Asp
ENST00000646985.1:c.3424A>G ENSP00000495053.1:p.Asn1142Asp
ENST00000647223.1:n.5960A>G
ENST00000651418.1:c.1869+1738A>G ENSP00000499150.1:n.1869+1738A>G
ENST00000306058.9:c.3592A>G ENSP00000305119.5:p.Asn1198Asp
ENST00000375687.8:c.3607A>G ENSP00000364839.4:p.Asn1203Asp
ENST00000613218.4:c.3607A>G ENSP00000480487.1:p.Asn1203Asp
ENST00000620121.4:c.3607A>G ENSP00000481978.1:p.Asn1203Asp
NM_015338.5:c.3607A>G , LRG_630t1:c.3607A>G NP_056153.2:p.Asn1203Asp
XM_006723727.2:c.3604A>G XP_006723790.1:p.Asn1202Asp
XM_006723728.2:c.3577A>G XP_006723791.1:p.Asn1193Asp
XM_006723730.2:c.3523A>G XP_006723793.1:p.Asn1175Asp
XM_006723732.2:c.3424A>G XP_006723795.1:p.Asn1142Asp
XM_006723733.1:c.2923A>G XP_006723796.1:p.Asn975Asp
XM_011528647.1:c.3871A>G XP_011526949.1:p.Asn1291Asp
XM_011528648.1:c.3868A>G XP_011526950.1:p.Asn1290Asp
XM_011528649.1:c.3787A>G XP_011526951.1:p.Asn1263Asp
XM_011528650.1:c.3718A>G XP_011526952.1:p.Asn1240Asp
XM_011528651.1:c.3586A>G XP_011526953.1:p.Asn1196Asp
XM_011528652.1:c.3523A>G XP_011526954.1:p.Asn1175Asp
NM_001363734.1:c.3424A>G NP_001350663.1:p.Asn1142Asp
XM_006723727.3:c.3604A>G XP_006723790.1:p.Asn1202Asp
XM_006723728.3:c.3577A>G XP_006723791.1:p.Asn1193Asp
XM_006723730.4:c.3523A>G XP_006723793.1:p.Asn1175Asp
XM_011528648.3:c.3868A>G XP_011526950.1:p.Asn1290Asp
XM_011528652.2:c.3523A>G XP_011526954.1:p.Asn1175Asp
XM_017027704.1:c.3523A>G XP_016883193.1:p.Asn1175Asp
XM_017027705.1:c.3523A>G XP_016883194.1:p.Asn1175Asp
XM_017027706.1:c.3454A>G XP_016883195.1:p.Asn1152Asp
NM_015338.6:c.3607A>G MANE Select NP_056153.2:p.Asn1203Asp