Canonical Allele Identifier: CA346074626

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965197A>C (hg19) ; chr2:g.25742328A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742328A>C , CM000664.2:g.25742328A>C	GRCh38
NC_000002.11:g.25965197A>C , CM000664.1:g.25965197A>C	GRCh37
NC_000002.10:g.25818701A>C	NCBI36
NG_052995.1:g.141189T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4006T>G	ENSP00000337250.5:p.Ser1336Ala
ENST00000435504.9:c.4009T>G MANE Select	ENSP00000391447.3:p.Ser1337Ala
ENST00000336112.8:c.3925T>G	ENSP00000337250.4:p.Ser1309Ala
ENST00000404843.5:c.2458T>G	ENSP00000383920.1:p.Ser820Ala
ENST00000435504.8:c.4009T>G	ENSP00000391447.3:p.Ser1337Ala
NM_018263.4:c.4009T>G	NP_060733.4:p.Ser1337Ala
XM_006712039.2:c.3643T>G	XP_006712102.1:p.Ser1215Ala
XM_006712040.1:c.3229T>G	XP_006712103.1:p.Ser1077Ala
XM_011532950.1:c.4006T>G	XP_011531252.1:p.Ser1336Ala
XM_011532951.1:c.3835T>G	XP_011531253.1:p.Ser1279Ala
NM_018263.5:c.4009T>G	NP_060733.4:p.Ser1337Ala
XM_006712039.3:c.3643T>G	XP_006712102.1:p.Ser1215Ala
XM_006712040.2:c.3229T>G	XP_006712103.1:p.Ser1077Ala
XM_011532950.3:c.4006T>G	XP_011531252.1:p.Ser1336Ala
XM_011532951.2:c.3835T>G	XP_011531253.1:p.Ser1279Ala
XM_017004430.1:c.3229T>G	XP_016859919.1:p.Ser1077Ala
XM_024452974.1:c.4189T>G	XP_024308742.1:p.Ser1397Ala
NM_001369346.1:c.3835T>G	NP_001356275.1:p.Ser1279Ala
NM_001369347.1:c.3229T>G	NP_001356276.1:p.Ser1077Ala
NM_018263.6:c.4009T>G MANE Select	NP_060733.4:p.Ser1337Ala