Canonical Allele Identifier: CA346074051

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965118G>T (hg19) ; chr2:g.25742249G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742249G>T , CM000664.2:g.25742249G>T	GRCh38
NC_000002.11:g.25965118G>T , CM000664.1:g.25965118G>T	GRCh37
NC_000002.10:g.25818622G>T	NCBI36
NG_052995.1:g.141268C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4085C>A	ENSP00000337250.5:p.Thr1362Asn
ENST00000435504.9:c.4088C>A MANE Select	ENSP00000391447.3:p.Thr1363Asn
ENST00000336112.8:c.4004C>A	ENSP00000337250.4:p.Thr1335Asn
ENST00000404843.5:c.2537C>A	ENSP00000383920.1:p.Thr846Asn
ENST00000435504.8:c.4088C>A	ENSP00000391447.3:p.Thr1363Asn
NM_018263.4:c.4088C>A	NP_060733.4:p.Thr1363Asn
XM_006712039.2:c.3722C>A	XP_006712102.1:p.Thr1241Asn
XM_006712040.1:c.3308C>A	XP_006712103.1:p.Thr1103Asn
XM_011532950.1:c.4085C>A	XP_011531252.1:p.Thr1362Asn
XM_011532951.1:c.3914C>A	XP_011531253.1:p.Thr1305Asn
NM_018263.5:c.4088C>A	NP_060733.4:p.Thr1363Asn
XM_006712039.3:c.3722C>A	XP_006712102.1:p.Thr1241Asn
XM_006712040.2:c.3308C>A	XP_006712103.1:p.Thr1103Asn
XM_011532950.3:c.4085C>A	XP_011531252.1:p.Thr1362Asn
XM_011532951.2:c.3914C>A	XP_011531253.1:p.Thr1305Asn
XM_017004430.1:c.3308C>A	XP_016859919.1:p.Thr1103Asn
XM_024452974.1:c.4268C>A	XP_024308742.1:p.Thr1423Asn
NM_001369346.1:c.3914C>A	NP_001356275.1:p.Thr1305Asn
NM_001369347.1:c.3308C>A	NP_001356276.1:p.Thr1103Asn
NM_018263.6:c.4088C>A MANE Select	NP_060733.4:p.Thr1363Asn