Canonical Allele Identifier: CA346073793

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965060A>C (hg19) ; chr2:g.25742191A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742191A>C , CM000664.2:g.25742191A>C	GRCh38
NC_000002.11:g.25965060A>C , CM000664.1:g.25965060A>C	GRCh37
NC_000002.10:g.25818564A>C	NCBI36
NG_052995.1:g.141326T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4143T>G	ENSP00000337250.5:p.Ile1381Met
ENST00000435504.9:c.4146T>G MANE Select	ENSP00000391447.3:p.Ile1382Met
ENST00000336112.8:c.4062T>G	ENSP00000337250.4:p.Ile1354Met
ENST00000404843.5:c.2595T>G	ENSP00000383920.1:p.Ile865Met
ENST00000435504.8:c.4146T>G	ENSP00000391447.3:p.Ile1382Met
NM_018263.4:c.4146T>G	NP_060733.4:p.Ile1382Met
XM_006712039.2:c.3780T>G	XP_006712102.1:p.Ile1260Met
XM_006712040.1:c.3366T>G	XP_006712103.1:p.Ile1122Met
XM_011532950.1:c.4143T>G	XP_011531252.1:p.Ile1381Met
XM_011532951.1:c.3972T>G	XP_011531253.1:p.Ile1324Met
NM_018263.5:c.4146T>G	NP_060733.4:p.Ile1382Met
XM_006712039.3:c.3780T>G	XP_006712102.1:p.Ile1260Met
XM_006712040.2:c.3366T>G	XP_006712103.1:p.Ile1122Met
XM_011532950.3:c.4143T>G	XP_011531252.1:p.Ile1381Met
XM_011532951.2:c.3972T>G	XP_011531253.1:p.Ile1324Met
XM_017004430.1:c.3366T>G	XP_016859919.1:p.Ile1122Met
XM_024452974.1:c.4326T>G	XP_024308742.1:p.Ile1442Met
NM_001369346.1:c.3972T>G	NP_001356275.1:p.Ile1324Met
NM_001369347.1:c.3366T>G	NP_001356276.1:p.Ile1122Met
NM_018263.6:c.4146T>G MANE Select	NP_060733.4:p.Ile1382Met