Canonical Allele Identifier: CA346076239

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965443T>G (hg19) ; chr2:g.25742574T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742574T>G , CM000664.2:g.25742574T>G	GRCh38
NC_000002.11:g.25965443T>G , CM000664.1:g.25965443T>G	GRCh37
NC_000002.10:g.25818947T>G	NCBI36
NG_052995.1:g.140943A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3760A>C	ENSP00000337250.5:p.Thr1254Pro
ENST00000435504.9:c.3763A>C MANE Select	ENSP00000391447.3:p.Thr1255Pro
ENST00000336112.8:c.3679A>C	ENSP00000337250.4:p.Thr1227Pro
ENST00000404843.5:c.2212A>C	ENSP00000383920.1:p.Thr738Pro
ENST00000435504.8:c.3763A>C	ENSP00000391447.3:p.Thr1255Pro
NM_018263.4:c.3763A>C	NP_060733.4:p.Thr1255Pro
XM_006712039.2:c.3397A>C	XP_006712102.1:p.Thr1133Pro
XM_006712040.1:c.2983A>C	XP_006712103.1:p.Thr995Pro
XM_011532950.1:c.3760A>C	XP_011531252.1:p.Thr1254Pro
XM_011532951.1:c.3589A>C	XP_011531253.1:p.Thr1197Pro
NM_018263.5:c.3763A>C	NP_060733.4:p.Thr1255Pro
XM_006712039.3:c.3397A>C	XP_006712102.1:p.Thr1133Pro
XM_006712040.2:c.2983A>C	XP_006712103.1:p.Thr995Pro
XM_011532950.3:c.3760A>C	XP_011531252.1:p.Thr1254Pro
XM_011532951.2:c.3589A>C	XP_011531253.1:p.Thr1197Pro
XM_017004430.1:c.2983A>C	XP_016859919.1:p.Thr995Pro
XM_024452974.1:c.3943A>C	XP_024308742.1:p.Thr1315Pro
NM_001369346.1:c.3589A>C	NP_001356275.1:p.Thr1197Pro
NM_001369347.1:c.2983A>C	NP_001356276.1:p.Thr995Pro
NM_018263.6:c.3763A>C MANE Select	NP_060733.4:p.Thr1255Pro