Canonical Allele Identifier: CA425353680

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965336A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742467A>G , CM000664.2:g.25742467A>G	GRCh38
NC_000002.11:g.25965336A>G , CM000664.1:g.25965336A>G	GRCh37
NC_000002.10:g.25818840A>G	NCBI36
NG_052995.1:g.141050T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3867T>C	ENSP00000337250.5:p.Ser1289=
ENST00000435504.9:c.3870T>C MANE Select	ENSP00000391447.3:p.Ser1290=
ENST00000336112.8:c.3786T>C	ENSP00000337250.4:p.Ser1262=
ENST00000404843.5:c.2319T>C	ENSP00000383920.1:p.Ser773=
ENST00000435504.8:c.3870T>C	ENSP00000391447.3:p.Ser1290=
NM_018263.4:c.3870T>C	NP_060733.4:p.Ser1290=
XM_006712039.2:c.3504T>C	XP_006712102.1:p.Ser1168=
XM_006712040.1:c.3090T>C	XP_006712103.1:p.Ser1030=
XM_011532950.1:c.3867T>C	XP_011531252.1:p.Ser1289=
XM_011532951.1:c.3696T>C	XP_011531253.1:p.Ser1232=
NM_018263.5:c.3870T>C	NP_060733.4:p.Ser1290=
XM_006712039.3:c.3504T>C	XP_006712102.1:p.Ser1168=
XM_006712040.2:c.3090T>C	XP_006712103.1:p.Ser1030=
XM_011532950.3:c.3867T>C	XP_011531252.1:p.Ser1289=
XM_011532951.2:c.3696T>C	XP_011531253.1:p.Ser1232=
XM_017004430.1:c.3090T>C	XP_016859919.1:p.Ser1030=
XM_024452974.1:c.4050T>C	XP_024308742.1:p.Ser1350=
NM_001369346.1:c.3696T>C	NP_001356275.1:p.Ser1232=
NM_001369347.1:c.3090T>C	NP_001356276.1:p.Ser1030=
NM_018263.6:c.3870T>C MANE Select	NP_060733.4:p.Ser1290=