Canonical Allele Identifier: CA346074929

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965236C>T (hg19) ; chr2:g.25742367C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742367C>T , CM000664.2:g.25742367C>T	GRCh38
NC_000002.11:g.25965236C>T , CM000664.1:g.25965236C>T	GRCh37
NC_000002.10:g.25818740C>T	NCBI36
NG_052995.1:g.141150G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3967G>A	ENSP00000337250.5:p.Gly1323Arg
ENST00000435504.9:c.3970G>A MANE Select	ENSP00000391447.3:p.Gly1324Arg
ENST00000336112.8:c.3886G>A	ENSP00000337250.4:p.Gly1296Arg
ENST00000404843.5:c.2419G>A	ENSP00000383920.1:p.Gly807Arg
ENST00000435504.8:c.3970G>A	ENSP00000391447.3:p.Gly1324Arg
NM_018263.4:c.3970G>A	NP_060733.4:p.Gly1324Arg
XM_006712039.2:c.3604G>A	XP_006712102.1:p.Gly1202Arg
XM_006712040.1:c.3190G>A	XP_006712103.1:p.Gly1064Arg
XM_011532950.1:c.3967G>A	XP_011531252.1:p.Gly1323Arg
XM_011532951.1:c.3796G>A	XP_011531253.1:p.Gly1266Arg
NM_018263.5:c.3970G>A	NP_060733.4:p.Gly1324Arg
XM_006712039.3:c.3604G>A	XP_006712102.1:p.Gly1202Arg
XM_006712040.2:c.3190G>A	XP_006712103.1:p.Gly1064Arg
XM_011532950.3:c.3967G>A	XP_011531252.1:p.Gly1323Arg
XM_011532951.2:c.3796G>A	XP_011531253.1:p.Gly1266Arg
XM_017004430.1:c.3190G>A	XP_016859919.1:p.Gly1064Arg
XM_024452974.1:c.4150G>A	XP_024308742.1:p.Gly1384Arg
NM_001369346.1:c.3796G>A	NP_001356275.1:p.Gly1266Arg
NM_001369347.1:c.3190G>A	NP_001356276.1:p.Gly1064Arg
NM_018263.6:c.3970G>A MANE Select	NP_060733.4:p.Gly1324Arg