Canonical Allele Identifier: CA346075681

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742493-T-C
• MyVariant Identifiers: chr2:g.25965362T>C (hg19) ; chr2:g.25742493T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742493T>C , CM000664.2:g.25742493T>C	GRCh38
NC_000002.11:g.25965362T>C , CM000664.1:g.25965362T>C	GRCh37
NC_000002.10:g.25818866T>C	NCBI36
NG_052995.1:g.141024A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3841A>G	ENSP00000337250.5:p.Ile1281Val
ENST00000435504.9:c.3844A>G MANE Select	ENSP00000391447.3:p.Ile1282Val
ENST00000336112.8:c.3760A>G	ENSP00000337250.4:p.Ile1254Val
ENST00000404843.5:c.2293A>G	ENSP00000383920.1:p.Ile765Val
ENST00000435504.8:c.3844A>G	ENSP00000391447.3:p.Ile1282Val
NM_018263.4:c.3844A>G	NP_060733.4:p.Ile1282Val
XM_006712039.2:c.3478A>G	XP_006712102.1:p.Ile1160Val
XM_006712040.1:c.3064A>G	XP_006712103.1:p.Ile1022Val
XM_011532950.1:c.3841A>G	XP_011531252.1:p.Ile1281Val
XM_011532951.1:c.3670A>G	XP_011531253.1:p.Ile1224Val
NM_018263.5:c.3844A>G	NP_060733.4:p.Ile1282Val
XM_006712039.3:c.3478A>G	XP_006712102.1:p.Ile1160Val
XM_006712040.2:c.3064A>G	XP_006712103.1:p.Ile1022Val
XM_011532950.3:c.3841A>G	XP_011531252.1:p.Ile1281Val
XM_011532951.2:c.3670A>G	XP_011531253.1:p.Ile1224Val
XM_017004430.1:c.3064A>G	XP_016859919.1:p.Ile1022Val
XM_024452974.1:c.4024A>G	XP_024308742.1:p.Ile1342Val
NM_001369346.1:c.3670A>G	NP_001356275.1:p.Ile1224Val
NM_001369347.1:c.3064A>G	NP_001356276.1:p.Ile1022Val
NM_018263.6:c.3844A>G MANE Select	NP_060733.4:p.Ile1282Val