Canonical Allele Identifier: CA1239490305

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742035_25742038delinsAACG , CM000664.2:g.25742035_25742038delinsAACG	GRCh38
NC_000002.11:g.25964904_25964907delinsAACG , CM000664.1:g.25964904_25964907delinsAACG	GRCh37
NC_000002.10:g.25818408_25818411delinsAACG	NCBI36
NG_052995.1:g.141479_141482delinsCGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4296_4299delinsCGTT	ENSP00000337250.5:p.Val1432=
ENST00000435504.9:c.4299_4302delinsCGTT MANE Select	ENSP00000391447.3:p.Val1433=
ENST00000336112.8:c.4215_4218delinsCGTT	ENSP00000337250.4:p.Val1405=
ENST00000404843.5:c.2748_2751delinsCGTT	ENSP00000383920.1:p.Val916=
ENST00000435504.8:c.4299_4302delinsCGTT	ENSP00000391447.3:p.Val1433=
NM_018263.4:c.4299_4302delinsCGTT	NP_060733.4:p.Val1433=
XM_006712039.2:c.3933_3936delinsCGTT	XP_006712102.1:p.Val1311=
XM_006712040.1:c.3519_3522delinsCGTT	XP_006712103.1:p.Val1173=
XM_011532950.1:c.4296_4299delinsCGTT	XP_011531252.1:p.Val1432=
XM_011532951.1:c.4125_4128delinsCGTT	XP_011531253.1:p.Val1375=
NM_018263.5:c.4299_4302delinsCGTT	NP_060733.4:p.Val1433=
XM_006712039.3:c.3933_3936delinsCGTT	XP_006712102.1:p.Val1311=
XM_006712040.2:c.3519_3522delinsCGTT	XP_006712103.1:p.Val1173=
XM_011532950.3:c.4296_4299delinsCGTT	XP_011531252.1:p.Val1432=
XM_011532951.2:c.4125_4128delinsCGTT	XP_011531253.1:p.Val1375=
XM_017004430.1:c.3519_3522delinsCGTT	XP_016859919.1:p.Val1173=
XM_024452974.1:c.4479_4482delinsCGTT	XP_024308742.1:p.Val1493=
NM_001369346.1:c.4125_4128delinsCGTT	NP_001356275.1:p.Val1375=
NM_001369347.1:c.3519_3522delinsCGTT	NP_001356276.1:p.Val1173=
NM_018263.6:c.4299_4302delinsCGTT MANE Select	NP_060733.4:p.Val1433=