Canonical Allele Identifier: CA346076222

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965440A>T (hg19) ; chr2:g.25742571A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742571A>T , CM000664.2:g.25742571A>T	GRCh38
NC_000002.11:g.25965440A>T , CM000664.1:g.25965440A>T	GRCh37
NC_000002.10:g.25818944A>T	NCBI36
NG_052995.1:g.140946T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3763T>A	ENSP00000337250.5:p.Phe1255Ile
ENST00000435504.9:c.3766T>A MANE Select	ENSP00000391447.3:p.Phe1256Ile
ENST00000336112.8:c.3682T>A	ENSP00000337250.4:p.Phe1228Ile
ENST00000404843.5:c.2215T>A	ENSP00000383920.1:p.Phe739Ile
ENST00000435504.8:c.3766T>A	ENSP00000391447.3:p.Phe1256Ile
NM_018263.4:c.3766T>A	NP_060733.4:p.Phe1256Ile
XM_006712039.2:c.3400T>A	XP_006712102.1:p.Phe1134Ile
XM_006712040.1:c.2986T>A	XP_006712103.1:p.Phe996Ile
XM_011532950.1:c.3763T>A	XP_011531252.1:p.Phe1255Ile
XM_011532951.1:c.3592T>A	XP_011531253.1:p.Phe1198Ile
NM_018263.5:c.3766T>A	NP_060733.4:p.Phe1256Ile
XM_006712039.3:c.3400T>A	XP_006712102.1:p.Phe1134Ile
XM_006712040.2:c.2986T>A	XP_006712103.1:p.Phe996Ile
XM_011532950.3:c.3763T>A	XP_011531252.1:p.Phe1255Ile
XM_011532951.2:c.3592T>A	XP_011531253.1:p.Phe1198Ile
XM_017004430.1:c.2986T>A	XP_016859919.1:p.Phe996Ile
XM_024452974.1:c.3946T>A	XP_024308742.1:p.Phe1316Ile
NM_001369346.1:c.3592T>A	NP_001356275.1:p.Phe1198Ile
NM_001369347.1:c.2986T>A	NP_001356276.1:p.Phe996Ile
NM_018263.6:c.3766T>A MANE Select	NP_060733.4:p.Phe1256Ile