Canonical Allele Identifier: CA346073522

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25964940G>C (hg19) ; chr2:g.25742071G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742071G>C , CM000664.2:g.25742071G>C	GRCh38
NC_000002.11:g.25964940G>C , CM000664.1:g.25964940G>C	GRCh37
NC_000002.10:g.25818444G>C	NCBI36
NG_052995.1:g.141446C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4263C>G	ENSP00000337250.5:p.Ile1421Met
ENST00000435504.9:c.4266C>G MANE Select	ENSP00000391447.3:p.Ile1422Met
ENST00000336112.8:c.4182C>G	ENSP00000337250.4:p.Ile1394Met
ENST00000404843.5:c.2715C>G	ENSP00000383920.1:p.Ile905Met
ENST00000435504.8:c.4266C>G	ENSP00000391447.3:p.Ile1422Met
NM_018263.4:c.4266C>G	NP_060733.4:p.Ile1422Met
XM_006712039.2:c.3900C>G	XP_006712102.1:p.Ile1300Met
XM_006712040.1:c.3486C>G	XP_006712103.1:p.Ile1162Met
XM_011532950.1:c.4263C>G	XP_011531252.1:p.Ile1421Met
XM_011532951.1:c.4092C>G	XP_011531253.1:p.Ile1364Met
NM_018263.5:c.4266C>G	NP_060733.4:p.Ile1422Met
XM_006712039.3:c.3900C>G	XP_006712102.1:p.Ile1300Met
XM_006712040.2:c.3486C>G	XP_006712103.1:p.Ile1162Met
XM_011532950.3:c.4263C>G	XP_011531252.1:p.Ile1421Met
XM_011532951.2:c.4092C>G	XP_011531253.1:p.Ile1364Met
XM_017004430.1:c.3486C>G	XP_016859919.1:p.Ile1162Met
XM_024452974.1:c.4446C>G	XP_024308742.1:p.Ile1482Met
NM_001369346.1:c.4092C>G	NP_001356275.1:p.Ile1364Met
NM_001369347.1:c.3486C>G	NP_001356276.1:p.Ile1162Met
NM_018263.6:c.4266C>G MANE Select	NP_060733.4:p.Ile1422Met