Canonical Allele Identifier: CA425354391

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965135G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742266G>T , CM000664.2:g.25742266G>T	GRCh38
NC_000002.11:g.25965135G>T , CM000664.1:g.25965135G>T	GRCh37
NC_000002.10:g.25818639G>T	NCBI36
NG_052995.1:g.141251C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4068C>A	ENSP00000337250.5:p.Val1356=
ENST00000435504.9:c.4071C>A MANE Select	ENSP00000391447.3:p.Val1357=
ENST00000336112.8:c.3987C>A	ENSP00000337250.4:p.Val1329=
ENST00000404843.5:c.2520C>A	ENSP00000383920.1:p.Val840=
ENST00000435504.8:c.4071C>A	ENSP00000391447.3:p.Val1357=
NM_018263.4:c.4071C>A	NP_060733.4:p.Val1357=
XM_006712039.2:c.3705C>A	XP_006712102.1:p.Val1235=
XM_006712040.1:c.3291C>A	XP_006712103.1:p.Val1097=
XM_011532950.1:c.4068C>A	XP_011531252.1:p.Val1356=
XM_011532951.1:c.3897C>A	XP_011531253.1:p.Val1299=
NM_018263.5:c.4071C>A	NP_060733.4:p.Val1357=
XM_006712039.3:c.3705C>A	XP_006712102.1:p.Val1235=
XM_006712040.2:c.3291C>A	XP_006712103.1:p.Val1097=
XM_011532950.3:c.4068C>A	XP_011531252.1:p.Val1356=
XM_011532951.2:c.3897C>A	XP_011531253.1:p.Val1299=
XM_017004430.1:c.3291C>A	XP_016859919.1:p.Val1097=
XM_024452974.1:c.4251C>A	XP_024308742.1:p.Val1417=
NM_001369346.1:c.3897C>A	NP_001356275.1:p.Val1299=
NM_001369347.1:c.3291C>A	NP_001356276.1:p.Val1097=
NM_018263.6:c.4071C>A MANE Select	NP_060733.4:p.Val1357=