Canonical Allele Identifier: CA346073613

Gene: ASXL2

Linked Data

• COSMIC: COSM225833 ; COSM225834
• MyVariant Identifiers: chr2:g.25964978A>T (hg19) ; chr2:g.25742109A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742109A>T , CM000664.2:g.25742109A>T	GRCh38
NC_000002.11:g.25964978A>T , CM000664.1:g.25964978A>T	GRCh37
NC_000002.10:g.25818482A>T	NCBI36
NG_052995.1:g.141408T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4225T>A	ENSP00000337250.5:p.Cys1409Ser
ENST00000435504.9:c.4228T>A MANE Select	ENSP00000391447.3:p.Cys1410Ser
ENST00000336112.8:c.4144T>A	ENSP00000337250.4:p.Cys1382Ser
ENST00000404843.5:c.2677T>A	ENSP00000383920.1:p.Cys893Ser
ENST00000435504.8:c.4228T>A	ENSP00000391447.3:p.Cys1410Ser
NM_018263.4:c.4228T>A	NP_060733.4:p.Cys1410Ser
XM_006712039.2:c.3862T>A	XP_006712102.1:p.Cys1288Ser
XM_006712040.1:c.3448T>A	XP_006712103.1:p.Cys1150Ser
XM_011532950.1:c.4225T>A	XP_011531252.1:p.Cys1409Ser
XM_011532951.1:c.4054T>A	XP_011531253.1:p.Cys1352Ser
NM_018263.5:c.4228T>A	NP_060733.4:p.Cys1410Ser
XM_006712039.3:c.3862T>A	XP_006712102.1:p.Cys1288Ser
XM_006712040.2:c.3448T>A	XP_006712103.1:p.Cys1150Ser
XM_011532950.3:c.4225T>A	XP_011531252.1:p.Cys1409Ser
XM_011532951.2:c.4054T>A	XP_011531253.1:p.Cys1352Ser
XM_017004430.1:c.3448T>A	XP_016859919.1:p.Cys1150Ser
XM_024452974.1:c.4408T>A	XP_024308742.1:p.Cys1470Ser
NM_001369346.1:c.4054T>A	NP_001356275.1:p.Cys1352Ser
NM_001369347.1:c.3448T>A	NP_001356276.1:p.Cys1150Ser
NM_018263.6:c.4228T>A MANE Select	NP_060733.4:p.Cys1410Ser