Canonical Allele Identifier: CA425181251

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742056-C-A
• MyVariant Identifiers: chr2:g.25964925C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742056C>A , CM000664.2:g.25742056C>A	GRCh38
NC_000002.11:g.25964925C>A , CM000664.1:g.25964925C>A	GRCh37
NC_000002.10:g.25818429C>A	NCBI36
NG_052995.1:g.141461G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4278G>T	ENSP00000337250.5:p.Leu1426=
ENST00000435504.9:c.4281G>T MANE Select	ENSP00000391447.3:p.Leu1427=
ENST00000336112.8:c.4197G>T	ENSP00000337250.4:p.Leu1399=
ENST00000404843.5:c.2730G>T	ENSP00000383920.1:p.Leu910=
ENST00000435504.8:c.4281G>T	ENSP00000391447.3:p.Leu1427=
NM_018263.4:c.4281G>T	NP_060733.4:p.Leu1427=
XM_006712039.2:c.3915G>T	XP_006712102.1:p.Leu1305=
XM_006712040.1:c.3501G>T	XP_006712103.1:p.Leu1167=
XM_011532950.1:c.4278G>T	XP_011531252.1:p.Leu1426=
XM_011532951.1:c.4107G>T	XP_011531253.1:p.Leu1369=
NM_018263.5:c.4281G>T	NP_060733.4:p.Leu1427=
XM_006712039.3:c.3915G>T	XP_006712102.1:p.Leu1305=
XM_006712040.2:c.3501G>T	XP_006712103.1:p.Leu1167=
XM_011532950.3:c.4278G>T	XP_011531252.1:p.Leu1426=
XM_011532951.2:c.4107G>T	XP_011531253.1:p.Leu1369=
XM_017004430.1:c.3501G>T	XP_016859919.1:p.Leu1167=
XM_024452974.1:c.4461G>T	XP_024308742.1:p.Leu1487=
NM_001369346.1:c.4107G>T	NP_001356275.1:p.Leu1369=
NM_001369347.1:c.3501G>T	NP_001356276.1:p.Leu1167=
NM_018263.6:c.4281G>T MANE Select	NP_060733.4:p.Leu1427=