Canonical Allele Identifier: CA408563079

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023962G>C (hg19) ; chr20:g.32436159G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436159G>C , CM000682.2:g.32436159G>C	GRCh38
NC_000020.10:g.31023962G>C , CM000682.1:g.31023962G>C	GRCh37
NC_000020.9:g.30487623G>C	NCBI36
NG_027868.1:g.82816G>C , LRG_630:g.82816G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3447G>C MANE Select	ENSP00000364839.4:p.Met1149Ile
ENST00000646985.1:c.3264G>C	ENSP00000495053.1:p.Met1088Ile
ENST00000647223.1:n.5800G>C
ENST00000651418.1:c.1869+1578G>C	ENSP00000499150.1:n.1869+1578G>C
ENST00000306058.9:c.3432G>C	ENSP00000305119.5:p.Met1144Ile
ENST00000375687.8:c.3447G>C	ENSP00000364839.4:p.Met1149Ile
ENST00000613218.4:c.3447G>C	ENSP00000480487.1:p.Met1149Ile
ENST00000620121.4:c.3447G>C	ENSP00000481978.1:p.Met1149Ile
NM_015338.5:c.3447G>C , LRG_630t1:c.3447G>C	NP_056153.2:p.Met1149Ile
XM_006723727.2:c.3444G>C	XP_006723790.1:p.Met1148Ile
XM_006723728.2:c.3417G>C	XP_006723791.1:p.Met1139Ile
XM_006723730.2:c.3363G>C	XP_006723793.1:p.Met1121Ile
XM_006723732.2:c.3264G>C	XP_006723795.1:p.Met1088Ile
XM_006723733.1:c.2763G>C	XP_006723796.1:p.Met921Ile
XM_011528647.1:c.3711G>C	XP_011526949.1:p.Met1237Ile
XM_011528648.1:c.3708G>C	XP_011526950.1:p.Met1236Ile
XM_011528649.1:c.3627G>C	XP_011526951.1:p.Met1209Ile
XM_011528650.1:c.3558G>C	XP_011526952.1:p.Met1186Ile
XM_011528651.1:c.3426G>C	XP_011526953.1:p.Met1142Ile
XM_011528652.1:c.3363G>C	XP_011526954.1:p.Met1121Ile
NM_001363734.1:c.3264G>C	NP_001350663.1:p.Met1088Ile
XM_006723727.3:c.3444G>C	XP_006723790.1:p.Met1148Ile
XM_006723728.3:c.3417G>C	XP_006723791.1:p.Met1139Ile
XM_006723730.4:c.3363G>C	XP_006723793.1:p.Met1121Ile
XM_011528648.3:c.3708G>C	XP_011526950.1:p.Met1236Ile
XM_011528652.2:c.3363G>C	XP_011526954.1:p.Met1121Ile
XM_017027704.1:c.3363G>C	XP_016883193.1:p.Met1121Ile
XM_017027705.1:c.3363G>C	XP_016883194.1:p.Met1121Ile
XM_017027706.1:c.3294G>C	XP_016883195.1:p.Met1098Ile
NM_015338.6:c.3447G>C MANE Select	NP_056153.2:p.Met1149Ile