Canonical Allele Identifier: CA346075583

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965349G>T (hg19) ; chr2:g.25742480G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742480G>T , CM000664.2:g.25742480G>T	GRCh38
NC_000002.11:g.25965349G>T , CM000664.1:g.25965349G>T	GRCh37
NC_000002.10:g.25818853G>T	NCBI36
NG_052995.1:g.141037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3854C>A	ENSP00000337250.5:p.Pro1285His
ENST00000435504.9:c.3857C>A MANE Select	ENSP00000391447.3:p.Pro1286His
ENST00000336112.8:c.3773C>A	ENSP00000337250.4:p.Pro1258His
ENST00000404843.5:c.2306C>A	ENSP00000383920.1:p.Pro769His
ENST00000435504.8:c.3857C>A	ENSP00000391447.3:p.Pro1286His
NM_018263.4:c.3857C>A	NP_060733.4:p.Pro1286His
XM_006712039.2:c.3491C>A	XP_006712102.1:p.Pro1164His
XM_006712040.1:c.3077C>A	XP_006712103.1:p.Pro1026His
XM_011532950.1:c.3854C>A	XP_011531252.1:p.Pro1285His
XM_011532951.1:c.3683C>A	XP_011531253.1:p.Pro1228His
NM_018263.5:c.3857C>A	NP_060733.4:p.Pro1286His
XM_006712039.3:c.3491C>A	XP_006712102.1:p.Pro1164His
XM_006712040.2:c.3077C>A	XP_006712103.1:p.Pro1026His
XM_011532950.3:c.3854C>A	XP_011531252.1:p.Pro1285His
XM_011532951.2:c.3683C>A	XP_011531253.1:p.Pro1228His
XM_017004430.1:c.3077C>A	XP_016859919.1:p.Pro1026His
XM_024452974.1:c.4037C>A	XP_024308742.1:p.Pro1346His
NM_001369346.1:c.3683C>A	NP_001356275.1:p.Pro1228His
NM_001369347.1:c.3077C>A	NP_001356276.1:p.Pro1026His
NM_018263.6:c.3857C>A MANE Select	NP_060733.4:p.Pro1286His