Canonical Allele Identifier: CA346073582

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25964965C>A (hg19) ; chr2:g.25742096C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742096C>A , CM000664.2:g.25742096C>A	GRCh38
NC_000002.11:g.25964965C>A , CM000664.1:g.25964965C>A	GRCh37
NC_000002.10:g.25818469C>A	NCBI36
NG_052995.1:g.141421G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4238G>T	ENSP00000337250.5:p.Gly1413Val
ENST00000435504.9:c.4241G>T MANE Select	ENSP00000391447.3:p.Gly1414Val
ENST00000336112.8:c.4157G>T	ENSP00000337250.4:p.Gly1386Val
ENST00000404843.5:c.2690G>T	ENSP00000383920.1:p.Gly897Val
ENST00000435504.8:c.4241G>T	ENSP00000391447.3:p.Gly1414Val
NM_018263.4:c.4241G>T	NP_060733.4:p.Gly1414Val
XM_006712039.2:c.3875G>T	XP_006712102.1:p.Gly1292Val
XM_006712040.1:c.3461G>T	XP_006712103.1:p.Gly1154Val
XM_011532950.1:c.4238G>T	XP_011531252.1:p.Gly1413Val
XM_011532951.1:c.4067G>T	XP_011531253.1:p.Gly1356Val
NM_018263.5:c.4241G>T	NP_060733.4:p.Gly1414Val
XM_006712039.3:c.3875G>T	XP_006712102.1:p.Gly1292Val
XM_006712040.2:c.3461G>T	XP_006712103.1:p.Gly1154Val
XM_011532950.3:c.4238G>T	XP_011531252.1:p.Gly1413Val
XM_011532951.2:c.4067G>T	XP_011531253.1:p.Gly1356Val
XM_017004430.1:c.3461G>T	XP_016859919.1:p.Gly1154Val
XM_024452974.1:c.4421G>T	XP_024308742.1:p.Gly1474Val
NM_001369346.1:c.4067G>T	NP_001356275.1:p.Gly1356Val
NM_001369347.1:c.3461G>T	NP_001356276.1:p.Gly1154Val
NM_018263.6:c.4241G>T MANE Select	NP_060733.4:p.Gly1414Val