Canonical Allele Identifier: CA1239490314

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742058G= , CM000664.2:g.25742058G=	GRCh38
NC_000002.11:g.25964927G= , CM000664.1:g.25964927G=	GRCh37
NC_000002.10:g.25818431G=	NCBI36
NG_052995.1:g.141459C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4276C=	ENSP00000337250.5:p.Leu1426=
ENST00000435504.9:c.4279C= MANE Select	ENSP00000391447.3:p.Leu1427=
ENST00000336112.8:c.4195C=	ENSP00000337250.4:p.Leu1399=
ENST00000404843.5:c.2728C=	ENSP00000383920.1:p.Leu910=
ENST00000435504.8:c.4279C=	ENSP00000391447.3:p.Leu1427=
NM_018263.4:c.4279C=	NP_060733.4:p.Leu1427=
XM_006712039.2:c.3913C=	XP_006712102.1:p.Leu1305=
XM_006712040.1:c.3499C=	XP_006712103.1:p.Leu1167=
XM_011532950.1:c.4276C=	XP_011531252.1:p.Leu1426=
XM_011532951.1:c.4105C=	XP_011531253.1:p.Leu1369=
NM_018263.5:c.4279C=	NP_060733.4:p.Leu1427=
XM_006712039.3:c.3913C=	XP_006712102.1:p.Leu1305=
XM_006712040.2:c.3499C=	XP_006712103.1:p.Leu1167=
XM_011532950.3:c.4276C=	XP_011531252.1:p.Leu1426=
XM_011532951.2:c.4105C=	XP_011531253.1:p.Leu1369=
XM_017004430.1:c.3499C=	XP_016859919.1:p.Leu1167=
XM_024452974.1:c.4459C=	XP_024308742.1:p.Leu1487=
NM_001369346.1:c.4105C=	NP_001356275.1:p.Leu1369=
NM_001369347.1:c.3499C=	NP_001356276.1:p.Leu1167=
NM_018263.6:c.4279C= MANE Select	NP_060733.4:p.Leu1427=