Canonical Allele Identifier: CA408562509

Gene: ASXL1

Linked Data

• dbSNP Id: rs2011821531
• gnomAD v3: 20-32435887-A-G
• gnomAD v4: 20-32435887-A-G
• MyVariant Identifiers: chr20:g.31023690A>G (hg19) ; chr20:g.32435887A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435887A>G , CM000682.2:g.32435887A>G	GRCh38
NC_000020.10:g.31023690A>G , CM000682.1:g.31023690A>G	GRCh37
NC_000020.9:g.30487351A>G	NCBI36
NG_027868.1:g.82544A>G , LRG_630:g.82544A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3175A>G MANE Select	ENSP00000364839.4:p.Met1059Val
ENST00000646985.1:c.2992A>G	ENSP00000495053.1:p.Met998Val
ENST00000647223.1:n.5528A>G
ENST00000651418.1:c.1869+1306A>G	ENSP00000499150.1:n.1869+1306A>G
ENST00000306058.9:c.3160A>G	ENSP00000305119.5:p.Met1054Val
ENST00000375687.8:c.3175A>G	ENSP00000364839.4:p.Met1059Val
ENST00000613218.4:c.3175A>G	ENSP00000480487.1:p.Met1059Val
ENST00000620121.4:c.3175A>G	ENSP00000481978.1:p.Met1059Val
NM_015338.5:c.3175A>G , LRG_630t1:c.3175A>G	NP_056153.2:p.Met1059Val
XM_006723727.2:c.3172A>G	XP_006723790.1:p.Met1058Val
XM_006723728.2:c.3145A>G	XP_006723791.1:p.Met1049Val
XM_006723730.2:c.3091A>G	XP_006723793.1:p.Met1031Val
XM_006723732.2:c.2992A>G	XP_006723795.1:p.Met998Val
XM_006723733.1:c.2491A>G	XP_006723796.1:p.Met831Val
XM_011528647.1:c.3439A>G	XP_011526949.1:p.Met1147Val
XM_011528648.1:c.3436A>G	XP_011526950.1:p.Met1146Val
XM_011528649.1:c.3355A>G	XP_011526951.1:p.Met1119Val
XM_011528650.1:c.3286A>G	XP_011526952.1:p.Met1096Val
XM_011528651.1:c.3154A>G	XP_011526953.1:p.Met1052Val
XM_011528652.1:c.3091A>G	XP_011526954.1:p.Met1031Val
NM_001363734.1:c.2992A>G	NP_001350663.1:p.Met998Val
XM_006723727.3:c.3172A>G	XP_006723790.1:p.Met1058Val
XM_006723728.3:c.3145A>G	XP_006723791.1:p.Met1049Val
XM_006723730.4:c.3091A>G	XP_006723793.1:p.Met1031Val
XM_011528648.3:c.3436A>G	XP_011526950.1:p.Met1146Val
XM_011528652.2:c.3091A>G	XP_011526954.1:p.Met1031Val
XM_017027704.1:c.3091A>G	XP_016883193.1:p.Met1031Val
XM_017027705.1:c.3091A>G	XP_016883194.1:p.Met1031Val
XM_017027706.1:c.3022A>G	XP_016883195.1:p.Met1008Val
NM_015338.6:c.3175A>G MANE Select	NP_056153.2:p.Met1059Val