Canonical Allele Identifier: CA408563364

Gene: ASXL1

Linked Data

• ClinVar Variation Id: 1923411
• ClinVar RCV Id: RCV002634579
• gnomAD v4: 20-32436295-C-T
• MyVariant Identifiers: chr20:g.31024098C>T (hg19) ; chr20:g.32436295C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436295C>T , CM000682.2:g.32436295C>T	GRCh38
NC_000020.10:g.31024098C>T , CM000682.1:g.31024098C>T	GRCh37
NC_000020.9:g.30487759C>T	NCBI36
NG_027868.1:g.82952C>T , LRG_630:g.82952C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3583C>T MANE Select	ENSP00000364839.4:p.Gln1195Ter
ENST00000646985.1:c.3400C>T	ENSP00000495053.1:p.Gln1134Ter
ENST00000647223.1:n.5936C>T
ENST00000651418.1:c.1869+1714C>T	ENSP00000499150.1:n.1869+1714C>T
ENST00000306058.9:c.3568C>T	ENSP00000305119.5:p.Gln1190Ter
ENST00000375687.8:c.3583C>T	ENSP00000364839.4:p.Gln1195Ter
ENST00000613218.4:c.3583C>T	ENSP00000480487.1:p.Gln1195Ter
ENST00000620121.4:c.3583C>T	ENSP00000481978.1:p.Gln1195Ter
NM_015338.5:c.3583C>T , LRG_630t1:c.3583C>T	NP_056153.2:p.Gln1195Ter
XM_006723727.2:c.3580C>T	XP_006723790.1:p.Gln1194Ter
XM_006723728.2:c.3553C>T	XP_006723791.1:p.Gln1185Ter
XM_006723730.2:c.3499C>T	XP_006723793.1:p.Gln1167Ter
XM_006723732.2:c.3400C>T	XP_006723795.1:p.Gln1134Ter
XM_006723733.1:c.2899C>T	XP_006723796.1:p.Gln967Ter
XM_011528647.1:c.3847C>T	XP_011526949.1:p.Gln1283Ter
XM_011528648.1:c.3844C>T	XP_011526950.1:p.Gln1282Ter
XM_011528649.1:c.3763C>T	XP_011526951.1:p.Gln1255Ter
XM_011528650.1:c.3694C>T	XP_011526952.1:p.Gln1232Ter
XM_011528651.1:c.3562C>T	XP_011526953.1:p.Gln1188Ter
XM_011528652.1:c.3499C>T	XP_011526954.1:p.Gln1167Ter
NM_001363734.1:c.3400C>T	NP_001350663.1:p.Gln1134Ter
XM_006723727.3:c.3580C>T	XP_006723790.1:p.Gln1194Ter
XM_006723728.3:c.3553C>T	XP_006723791.1:p.Gln1185Ter
XM_006723730.4:c.3499C>T	XP_006723793.1:p.Gln1167Ter
XM_011528648.3:c.3844C>T	XP_011526950.1:p.Gln1282Ter
XM_011528652.2:c.3499C>T	XP_011526954.1:p.Gln1167Ter
XM_017027704.1:c.3499C>T	XP_016883193.1:p.Gln1167Ter
XM_017027705.1:c.3499C>T	XP_016883194.1:p.Gln1167Ter
XM_017027706.1:c.3430C>T	XP_016883195.1:p.Gln1144Ter
NM_015338.6:c.3583C>T MANE Select	NP_056153.2:p.Gln1195Ter