Canonical Allele Identifier: CA346073998

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965106A>T (hg19) ; chr2:g.25742237A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742237A>T , CM000664.2:g.25742237A>T	GRCh38
NC_000002.11:g.25965106A>T , CM000664.1:g.25965106A>T	GRCh37
NC_000002.10:g.25818610A>T	NCBI36
NG_052995.1:g.141280T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4097T>A	ENSP00000337250.5:p.Ile1366Asn
ENST00000435504.9:c.4100T>A MANE Select	ENSP00000391447.3:p.Ile1367Asn
ENST00000336112.8:c.4016T>A	ENSP00000337250.4:p.Ile1339Asn
ENST00000404843.5:c.2549T>A	ENSP00000383920.1:p.Ile850Asn
ENST00000435504.8:c.4100T>A	ENSP00000391447.3:p.Ile1367Asn
NM_018263.4:c.4100T>A	NP_060733.4:p.Ile1367Asn
XM_006712039.2:c.3734T>A	XP_006712102.1:p.Ile1245Asn
XM_006712040.1:c.3320T>A	XP_006712103.1:p.Ile1107Asn
XM_011532950.1:c.4097T>A	XP_011531252.1:p.Ile1366Asn
XM_011532951.1:c.3926T>A	XP_011531253.1:p.Ile1309Asn
NM_018263.5:c.4100T>A	NP_060733.4:p.Ile1367Asn
XM_006712039.3:c.3734T>A	XP_006712102.1:p.Ile1245Asn
XM_006712040.2:c.3320T>A	XP_006712103.1:p.Ile1107Asn
XM_011532950.3:c.4097T>A	XP_011531252.1:p.Ile1366Asn
XM_011532951.2:c.3926T>A	XP_011531253.1:p.Ile1309Asn
XM_017004430.1:c.3320T>A	XP_016859919.1:p.Ile1107Asn
XM_024452974.1:c.4280T>A	XP_024308742.1:p.Ile1427Asn
NM_001369346.1:c.3926T>A	NP_001356275.1:p.Ile1309Asn
NM_001369347.1:c.3320T>A	NP_001356276.1:p.Ile1107Asn
NM_018263.6:c.4100T>A MANE Select	NP_060733.4:p.Ile1367Asn