Canonical Allele Identifier: CA425181344

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965021G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742152G>A , CM000664.2:g.25742152G>A	GRCh38
NC_000002.11:g.25965021G>A , CM000664.1:g.25965021G>A	GRCh37
NC_000002.10:g.25818525G>A	NCBI36
NG_052995.1:g.141365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4182C>T	ENSP00000337250.5:p.Gly1394=
ENST00000435504.9:c.4185C>T MANE Select	ENSP00000391447.3:p.Gly1395=
ENST00000336112.8:c.4101C>T	ENSP00000337250.4:p.Gly1367=
ENST00000404843.5:c.2634C>T	ENSP00000383920.1:p.Gly878=
ENST00000435504.8:c.4185C>T	ENSP00000391447.3:p.Gly1395=
NM_018263.4:c.4185C>T	NP_060733.4:p.Gly1395=
XM_006712039.2:c.3819C>T	XP_006712102.1:p.Gly1273=
XM_006712040.1:c.3405C>T	XP_006712103.1:p.Gly1135=
XM_011532950.1:c.4182C>T	XP_011531252.1:p.Gly1394=
XM_011532951.1:c.4011C>T	XP_011531253.1:p.Gly1337=
NM_018263.5:c.4185C>T	NP_060733.4:p.Gly1395=
XM_006712039.3:c.3819C>T	XP_006712102.1:p.Gly1273=
XM_006712040.2:c.3405C>T	XP_006712103.1:p.Gly1135=
XM_011532950.3:c.4182C>T	XP_011531252.1:p.Gly1394=
XM_011532951.2:c.4011C>T	XP_011531253.1:p.Gly1337=
XM_017004430.1:c.3405C>T	XP_016859919.1:p.Gly1135=
XM_024452974.1:c.4365C>T	XP_024308742.1:p.Gly1455=
NM_001369346.1:c.4011C>T	NP_001356275.1:p.Gly1337=
NM_001369347.1:c.3405C>T	NP_001356276.1:p.Gly1135=
NM_018263.6:c.4185C>T MANE Select	NP_060733.4:p.Gly1395=