Canonical Allele Identifier: CA425181372

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965054A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742185A>C , CM000664.2:g.25742185A>C	GRCh38
NC_000002.11:g.25965054A>C , CM000664.1:g.25965054A>C	GRCh37
NC_000002.10:g.25818558A>C	NCBI36
NG_052995.1:g.141332T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4149T>G	ENSP00000337250.5:p.Val1383=
ENST00000435504.9:c.4152T>G MANE Select	ENSP00000391447.3:p.Val1384=
ENST00000336112.8:c.4068T>G	ENSP00000337250.4:p.Val1356=
ENST00000404843.5:c.2601T>G	ENSP00000383920.1:p.Val867=
ENST00000435504.8:c.4152T>G	ENSP00000391447.3:p.Val1384=
NM_018263.4:c.4152T>G	NP_060733.4:p.Val1384=
XM_006712039.2:c.3786T>G	XP_006712102.1:p.Val1262=
XM_006712040.1:c.3372T>G	XP_006712103.1:p.Val1124=
XM_011532950.1:c.4149T>G	XP_011531252.1:p.Val1383=
XM_011532951.1:c.3978T>G	XP_011531253.1:p.Val1326=
NM_018263.5:c.4152T>G	NP_060733.4:p.Val1384=
XM_006712039.3:c.3786T>G	XP_006712102.1:p.Val1262=
XM_006712040.2:c.3372T>G	XP_006712103.1:p.Val1124=
XM_011532950.3:c.4149T>G	XP_011531252.1:p.Val1383=
XM_011532951.2:c.3978T>G	XP_011531253.1:p.Val1326=
XM_017004430.1:c.3372T>G	XP_016859919.1:p.Val1124=
XM_024452974.1:c.4332T>G	XP_024308742.1:p.Val1444=
NM_001369346.1:c.3978T>G	NP_001356275.1:p.Val1326=
NM_001369347.1:c.3372T>G	NP_001356276.1:p.Val1124=
NM_018263.6:c.4152T>G MANE Select	NP_060733.4:p.Val1384=