Canonical Allele Identifier: CA346073628

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25964984T>G (hg19) ; chr2:g.25742115T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742115T>G , CM000664.2:g.25742115T>G	GRCh38
NC_000002.11:g.25964984T>G , CM000664.1:g.25964984T>G	GRCh37
NC_000002.10:g.25818488T>G	NCBI36
NG_052995.1:g.141402A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4219A>C	ENSP00000337250.5:p.Ile1407Leu
ENST00000435504.9:c.4222A>C MANE Select	ENSP00000391447.3:p.Ile1408Leu
ENST00000336112.8:c.4138A>C	ENSP00000337250.4:p.Ile1380Leu
ENST00000404843.5:c.2671A>C	ENSP00000383920.1:p.Ile891Leu
ENST00000435504.8:c.4222A>C	ENSP00000391447.3:p.Ile1408Leu
NM_018263.4:c.4222A>C	NP_060733.4:p.Ile1408Leu
XM_006712039.2:c.3856A>C	XP_006712102.1:p.Ile1286Leu
XM_006712040.1:c.3442A>C	XP_006712103.1:p.Ile1148Leu
XM_011532950.1:c.4219A>C	XP_011531252.1:p.Ile1407Leu
XM_011532951.1:c.4048A>C	XP_011531253.1:p.Ile1350Leu
NM_018263.5:c.4222A>C	NP_060733.4:p.Ile1408Leu
XM_006712039.3:c.3856A>C	XP_006712102.1:p.Ile1286Leu
XM_006712040.2:c.3442A>C	XP_006712103.1:p.Ile1148Leu
XM_011532950.3:c.4219A>C	XP_011531252.1:p.Ile1407Leu
XM_011532951.2:c.4048A>C	XP_011531253.1:p.Ile1350Leu
XM_017004430.1:c.3442A>C	XP_016859919.1:p.Ile1148Leu
XM_024452974.1:c.4402A>C	XP_024308742.1:p.Ile1468Leu
NM_001369346.1:c.4048A>C	NP_001356275.1:p.Ile1350Leu
NM_001369347.1:c.3442A>C	NP_001356276.1:p.Ile1148Leu
NM_018263.6:c.4222A>C MANE Select	NP_060733.4:p.Ile1408Leu