Canonical Allele Identifier: CA425353741

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965441T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742572T>G , CM000664.2:g.25742572T>G	GRCh38
NC_000002.11:g.25965441T>G , CM000664.1:g.25965441T>G	GRCh37
NC_000002.10:g.25818945T>G	NCBI36
NG_052995.1:g.140945A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3762A>C	ENSP00000337250.5:p.Thr1254=
ENST00000435504.9:c.3765A>C MANE Select	ENSP00000391447.3:p.Thr1255=
ENST00000336112.8:c.3681A>C	ENSP00000337250.4:p.Thr1227=
ENST00000404843.5:c.2214A>C	ENSP00000383920.1:p.Thr738=
ENST00000435504.8:c.3765A>C	ENSP00000391447.3:p.Thr1255=
NM_018263.4:c.3765A>C	NP_060733.4:p.Thr1255=
XM_006712039.2:c.3399A>C	XP_006712102.1:p.Thr1133=
XM_006712040.1:c.2985A>C	XP_006712103.1:p.Thr995=
XM_011532950.1:c.3762A>C	XP_011531252.1:p.Thr1254=
XM_011532951.1:c.3591A>C	XP_011531253.1:p.Thr1197=
NM_018263.5:c.3765A>C	NP_060733.4:p.Thr1255=
XM_006712039.3:c.3399A>C	XP_006712102.1:p.Thr1133=
XM_006712040.2:c.2985A>C	XP_006712103.1:p.Thr995=
XM_011532950.3:c.3762A>C	XP_011531252.1:p.Thr1254=
XM_011532951.2:c.3591A>C	XP_011531253.1:p.Thr1197=
XM_017004430.1:c.2985A>C	XP_016859919.1:p.Thr995=
XM_024452974.1:c.3945A>C	XP_024308742.1:p.Thr1315=
NM_001369346.1:c.3591A>C	NP_001356275.1:p.Thr1197=
NM_001369347.1:c.2985A>C	NP_001356276.1:p.Thr995=
NM_018263.6:c.3765A>C MANE Select	NP_060733.4:p.Thr1255=