Canonical Allele Identifier: CA346075964

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965401C>G (hg19) ; chr2:g.25742532C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742532C>G , CM000664.2:g.25742532C>G	GRCh38
NC_000002.11:g.25965401C>G , CM000664.1:g.25965401C>G	GRCh37
NC_000002.10:g.25818905C>G	NCBI36
NG_052995.1:g.140985G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3802G>C	ENSP00000337250.5:p.Ala1268Pro
ENST00000435504.9:c.3805G>C MANE Select	ENSP00000391447.3:p.Ala1269Pro
ENST00000336112.8:c.3721G>C	ENSP00000337250.4:p.Ala1241Pro
ENST00000404843.5:c.2254G>C	ENSP00000383920.1:p.Ala752Pro
ENST00000435504.8:c.3805G>C	ENSP00000391447.3:p.Ala1269Pro
NM_018263.4:c.3805G>C	NP_060733.4:p.Ala1269Pro
XM_006712039.2:c.3439G>C	XP_006712102.1:p.Ala1147Pro
XM_006712040.1:c.3025G>C	XP_006712103.1:p.Ala1009Pro
XM_011532950.1:c.3802G>C	XP_011531252.1:p.Ala1268Pro
XM_011532951.1:c.3631G>C	XP_011531253.1:p.Ala1211Pro
NM_018263.5:c.3805G>C	NP_060733.4:p.Ala1269Pro
XM_006712039.3:c.3439G>C	XP_006712102.1:p.Ala1147Pro
XM_006712040.2:c.3025G>C	XP_006712103.1:p.Ala1009Pro
XM_011532950.3:c.3802G>C	XP_011531252.1:p.Ala1268Pro
XM_011532951.2:c.3631G>C	XP_011531253.1:p.Ala1211Pro
XM_017004430.1:c.3025G>C	XP_016859919.1:p.Ala1009Pro
XM_024452974.1:c.3985G>C	XP_024308742.1:p.Ala1329Pro
NM_001369346.1:c.3631G>C	NP_001356275.1:p.Ala1211Pro
NM_001369347.1:c.3025G>C	NP_001356276.1:p.Ala1009Pro
NM_018263.6:c.3805G>C MANE Select	NP_060733.4:p.Ala1269Pro