Canonical Allele Identifier: CA346074697

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742339-A-C
• MyVariant Identifiers: chr2:g.25965208A>C (hg19) ; chr2:g.25742339A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742339A>C , CM000664.2:g.25742339A>C	GRCh38
NC_000002.11:g.25965208A>C , CM000664.1:g.25965208A>C	GRCh37
NC_000002.10:g.25818712A>C	NCBI36
NG_052995.1:g.141178T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3995T>G	ENSP00000337250.5:p.Val1332Gly
ENST00000435504.9:c.3998T>G MANE Select	ENSP00000391447.3:p.Val1333Gly
ENST00000336112.8:c.3914T>G	ENSP00000337250.4:p.Val1305Gly
ENST00000404843.5:c.2447T>G	ENSP00000383920.1:p.Val816Gly
ENST00000435504.8:c.3998T>G	ENSP00000391447.3:p.Val1333Gly
NM_018263.4:c.3998T>G	NP_060733.4:p.Val1333Gly
XM_006712039.2:c.3632T>G	XP_006712102.1:p.Val1211Gly
XM_006712040.1:c.3218T>G	XP_006712103.1:p.Val1073Gly
XM_011532950.1:c.3995T>G	XP_011531252.1:p.Val1332Gly
XM_011532951.1:c.3824T>G	XP_011531253.1:p.Val1275Gly
NM_018263.5:c.3998T>G	NP_060733.4:p.Val1333Gly
XM_006712039.3:c.3632T>G	XP_006712102.1:p.Val1211Gly
XM_006712040.2:c.3218T>G	XP_006712103.1:p.Val1073Gly
XM_011532950.3:c.3995T>G	XP_011531252.1:p.Val1332Gly
XM_011532951.2:c.3824T>G	XP_011531253.1:p.Val1275Gly
XM_017004430.1:c.3218T>G	XP_016859919.1:p.Val1073Gly
XM_024452974.1:c.4178T>G	XP_024308742.1:p.Val1393Gly
NM_001369346.1:c.3824T>G	NP_001356275.1:p.Val1275Gly
NM_001369347.1:c.3218T>G	NP_001356276.1:p.Val1073Gly
NM_018263.6:c.3998T>G MANE Select	NP_060733.4:p.Val1333Gly