Canonical Allele Identifier: CA346073778

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742183-T-C
• MyVariant Identifiers: chr2:g.25965052T>C (hg19) ; chr2:g.25742183T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742183T>C , CM000664.2:g.25742183T>C	GRCh38
NC_000002.11:g.25965052T>C , CM000664.1:g.25965052T>C	GRCh37
NC_000002.10:g.25818556T>C	NCBI36
NG_052995.1:g.141334A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4151A>G	ENSP00000337250.5:p.Gln1384Arg
ENST00000435504.9:c.4154A>G MANE Select	ENSP00000391447.3:p.Gln1385Arg
ENST00000336112.8:c.4070A>G	ENSP00000337250.4:p.Gln1357Arg
ENST00000404843.5:c.2603A>G	ENSP00000383920.1:p.Gln868Arg
ENST00000435504.8:c.4154A>G	ENSP00000391447.3:p.Gln1385Arg
NM_018263.4:c.4154A>G	NP_060733.4:p.Gln1385Arg
XM_006712039.2:c.3788A>G	XP_006712102.1:p.Gln1263Arg
XM_006712040.1:c.3374A>G	XP_006712103.1:p.Gln1125Arg
XM_011532950.1:c.4151A>G	XP_011531252.1:p.Gln1384Arg
XM_011532951.1:c.3980A>G	XP_011531253.1:p.Gln1327Arg
NM_018263.5:c.4154A>G	NP_060733.4:p.Gln1385Arg
XM_006712039.3:c.3788A>G	XP_006712102.1:p.Gln1263Arg
XM_006712040.2:c.3374A>G	XP_006712103.1:p.Gln1125Arg
XM_011532950.3:c.4151A>G	XP_011531252.1:p.Gln1384Arg
XM_011532951.2:c.3980A>G	XP_011531253.1:p.Gln1327Arg
XM_017004430.1:c.3374A>G	XP_016859919.1:p.Gln1125Arg
XM_024452974.1:c.4334A>G	XP_024308742.1:p.Gln1445Arg
NM_001369346.1:c.3980A>G	NP_001356275.1:p.Gln1327Arg
NM_001369347.1:c.3374A>G	NP_001356276.1:p.Gln1125Arg
NM_018263.6:c.4154A>G MANE Select	NP_060733.4:p.Gln1385Arg