Canonical Allele Identifier: CA1239490370

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742222G= , CM000664.2:g.25742222G=	GRCh38
NC_000002.11:g.25965091G= , CM000664.1:g.25965091G=	GRCh37
NC_000002.10:g.25818595G=	NCBI36
NG_052995.1:g.141295C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4112C=	ENSP00000337250.5:p.Ala1371=
ENST00000435504.9:c.4115C= MANE Select	ENSP00000391447.3:p.Ala1372=
ENST00000336112.8:c.4031C=	ENSP00000337250.4:p.Ala1344=
ENST00000404843.5:c.2564C=	ENSP00000383920.1:p.Ala855=
ENST00000435504.8:c.4115C=	ENSP00000391447.3:p.Ala1372=
NM_018263.4:c.4115C=	NP_060733.4:p.Ala1372=
XM_006712039.2:c.3749C=	XP_006712102.1:p.Ala1250=
XM_006712040.1:c.3335C=	XP_006712103.1:p.Ala1112=
XM_011532950.1:c.4112C=	XP_011531252.1:p.Ala1371=
XM_011532951.1:c.3941C=	XP_011531253.1:p.Ala1314=
NM_018263.5:c.4115C=	NP_060733.4:p.Ala1372=
XM_006712039.3:c.3749C=	XP_006712102.1:p.Ala1250=
XM_006712040.2:c.3335C=	XP_006712103.1:p.Ala1112=
XM_011532950.3:c.4112C=	XP_011531252.1:p.Ala1371=
XM_011532951.2:c.3941C=	XP_011531253.1:p.Ala1314=
XM_017004430.1:c.3335C=	XP_016859919.1:p.Ala1112=
XM_024452974.1:c.4295C=	XP_024308742.1:p.Ala1432=
NM_001369346.1:c.3941C=	NP_001356275.1:p.Ala1314=
NM_001369347.1:c.3335C=	NP_001356276.1:p.Ala1112=
NM_018263.6:c.4115C= MANE Select	NP_060733.4:p.Ala1372=