Canonical Allele Identifier: CA425353692

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965360G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742491G>A , CM000664.2:g.25742491G>A	GRCh38
NC_000002.11:g.25965360G>A , CM000664.1:g.25965360G>A	GRCh37
NC_000002.10:g.25818864G>A	NCBI36
NG_052995.1:g.141026C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3843C>T	ENSP00000337250.5:p.Ile1281=
ENST00000435504.9:c.3846C>T MANE Select	ENSP00000391447.3:p.Ile1282=
ENST00000336112.8:c.3762C>T	ENSP00000337250.4:p.Ile1254=
ENST00000404843.5:c.2295C>T	ENSP00000383920.1:p.Ile765=
ENST00000435504.8:c.3846C>T	ENSP00000391447.3:p.Ile1282=
NM_018263.4:c.3846C>T	NP_060733.4:p.Ile1282=
XM_006712039.2:c.3480C>T	XP_006712102.1:p.Ile1160=
XM_006712040.1:c.3066C>T	XP_006712103.1:p.Ile1022=
XM_011532950.1:c.3843C>T	XP_011531252.1:p.Ile1281=
XM_011532951.1:c.3672C>T	XP_011531253.1:p.Ile1224=
NM_018263.5:c.3846C>T	NP_060733.4:p.Ile1282=
XM_006712039.3:c.3480C>T	XP_006712102.1:p.Ile1160=
XM_006712040.2:c.3066C>T	XP_006712103.1:p.Ile1022=
XM_011532950.3:c.3843C>T	XP_011531252.1:p.Ile1281=
XM_011532951.2:c.3672C>T	XP_011531253.1:p.Ile1224=
XM_017004430.1:c.3066C>T	XP_016859919.1:p.Ile1022=
XM_024452974.1:c.4026C>T	XP_024308742.1:p.Ile1342=
NM_001369346.1:c.3672C>T	NP_001356275.1:p.Ile1224=
NM_001369347.1:c.3066C>T	NP_001356276.1:p.Ile1022=
NM_018263.6:c.3846C>T MANE Select	NP_060733.4:p.Ile1282=