Canonical Allele Identifier: CA9807946

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32358772A>G , CM000682.2:g.32358772A>G	GRCh38
NC_000020.10:g.30946575A>G , CM000682.1:g.30946575A>G	GRCh37
NC_000020.9:g.30410236A>G	NCBI36
NG_027868.1:g.5429A>G , LRG_630:g.5429A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.-4A>G MANE Select	ENSP00000364839.4:n.-4A>G
ENST00000644587.1:c.-4A>G	ENSP00000494813.1:n.-4A>G
ENST00000645337.1:c.-4A>G	ENSP00000494077.1:n.-4A>G
ENST00000646367.1:c.-4A>G	ENSP00000493987.1:n.-4A>G
ENST00000651418.1:c.-4A>G	ENSP00000499150.1:n.-4A>G
ENST00000375687.8:c.-4A>G	ENSP00000364839.4:n.-4A>G
ENST00000542461.5:c.-4A>G	ENSP00000438654.2:n.-4A>G
ENST00000613218.4:c.-4A>G	ENSP00000480487.1:n.-4A>G
ENST00000620121.4:c.-4A>G	ENSP00000481978.1:n.-4A>G
NM_001164603.1:c.-4A>G , LRG_630t2:c.-4A>G	NP_001158075.1:n.-4A>G
NM_015338.5:c.-4A>G , LRG_630t1:c.-4A>G	NP_056153.2:n.-4A>G
XM_006723727.2:c.-4A>G	XP_006723790.1:n.-4A>G
XM_006723727.3:c.-4A>G	XP_006723790.1:n.-4A>G
XM_017027706.1:c.-4A>G	XP_016883195.1:n.-4A>G
NM_015338.6:c.-4A>G MANE Select	NP_056153.2:n.-4A>G