Canonical Allele Identifier: CA346075771

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965376A>C (hg19) ; chr2:g.25742507A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742507A>C , CM000664.2:g.25742507A>C	GRCh38
NC_000002.11:g.25965376A>C , CM000664.1:g.25965376A>C	GRCh37
NC_000002.10:g.25818880A>C	NCBI36
NG_052995.1:g.141010T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3827T>G	ENSP00000337250.5:p.Val1276Gly
ENST00000435504.9:c.3830T>G MANE Select	ENSP00000391447.3:p.Val1277Gly
ENST00000336112.8:c.3746T>G	ENSP00000337250.4:p.Val1249Gly
ENST00000404843.5:c.2279T>G	ENSP00000383920.1:p.Val760Gly
ENST00000435504.8:c.3830T>G	ENSP00000391447.3:p.Val1277Gly
NM_018263.4:c.3830T>G	NP_060733.4:p.Val1277Gly
XM_006712039.2:c.3464T>G	XP_006712102.1:p.Val1155Gly
XM_006712040.1:c.3050T>G	XP_006712103.1:p.Val1017Gly
XM_011532950.1:c.3827T>G	XP_011531252.1:p.Val1276Gly
XM_011532951.1:c.3656T>G	XP_011531253.1:p.Val1219Gly
NM_018263.5:c.3830T>G	NP_060733.4:p.Val1277Gly
XM_006712039.3:c.3464T>G	XP_006712102.1:p.Val1155Gly
XM_006712040.2:c.3050T>G	XP_006712103.1:p.Val1017Gly
XM_011532950.3:c.3827T>G	XP_011531252.1:p.Val1276Gly
XM_011532951.2:c.3656T>G	XP_011531253.1:p.Val1219Gly
XM_017004430.1:c.3050T>G	XP_016859919.1:p.Val1017Gly
XM_024452974.1:c.4010T>G	XP_024308742.1:p.Val1337Gly
NM_001369346.1:c.3656T>G	NP_001356275.1:p.Val1219Gly
NM_001369347.1:c.3050T>G	NP_001356276.1:p.Val1017Gly
NM_018263.6:c.3830T>G MANE Select	NP_060733.4:p.Val1277Gly