Canonical Allele Identifier: CA346075484

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965328A>T (hg19) ; chr2:g.25742459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742459A>T , CM000664.2:g.25742459A>T	GRCh38
NC_000002.11:g.25965328A>T , CM000664.1:g.25965328A>T	GRCh37
NC_000002.10:g.25818832A>T	NCBI36
NG_052995.1:g.141058T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3875T>A	ENSP00000337250.5:p.Val1292Asp
ENST00000435504.9:c.3878T>A MANE Select	ENSP00000391447.3:p.Val1293Asp
ENST00000336112.8:c.3794T>A	ENSP00000337250.4:p.Val1265Asp
ENST00000404843.5:c.2327T>A	ENSP00000383920.1:p.Val776Asp
ENST00000435504.8:c.3878T>A	ENSP00000391447.3:p.Val1293Asp
NM_018263.4:c.3878T>A	NP_060733.4:p.Val1293Asp
XM_006712039.2:c.3512T>A	XP_006712102.1:p.Val1171Asp
XM_006712040.1:c.3098T>A	XP_006712103.1:p.Val1033Asp
XM_011532950.1:c.3875T>A	XP_011531252.1:p.Val1292Asp
XM_011532951.1:c.3704T>A	XP_011531253.1:p.Val1235Asp
NM_018263.5:c.3878T>A	NP_060733.4:p.Val1293Asp
XM_006712039.3:c.3512T>A	XP_006712102.1:p.Val1171Asp
XM_006712040.2:c.3098T>A	XP_006712103.1:p.Val1033Asp
XM_011532950.3:c.3875T>A	XP_011531252.1:p.Val1292Asp
XM_011532951.2:c.3704T>A	XP_011531253.1:p.Val1235Asp
XM_017004430.1:c.3098T>A	XP_016859919.1:p.Val1033Asp
XM_024452974.1:c.4058T>A	XP_024308742.1:p.Val1353Asp
NM_001369346.1:c.3704T>A	NP_001356275.1:p.Val1235Asp
NM_001369347.1:c.3098T>A	NP_001356276.1:p.Val1033Asp
NM_018263.6:c.3878T>A MANE Select	NP_060733.4:p.Val1293Asp