Canonical Allele Identifier: CA346075830

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965385G>T (hg19) ; chr2:g.25742516G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742516G>T , CM000664.2:g.25742516G>T	GRCh38
NC_000002.11:g.25965385G>T , CM000664.1:g.25965385G>T	GRCh37
NC_000002.10:g.25818889G>T	NCBI36
NG_052995.1:g.141001C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3818C>A	ENSP00000337250.5:p.Ala1273Asp
ENST00000435504.9:c.3821C>A MANE Select	ENSP00000391447.3:p.Ala1274Asp
ENST00000336112.8:c.3737C>A	ENSP00000337250.4:p.Ala1246Asp
ENST00000404843.5:c.2270C>A	ENSP00000383920.1:p.Ala757Asp
ENST00000435504.8:c.3821C>A	ENSP00000391447.3:p.Ala1274Asp
NM_018263.4:c.3821C>A	NP_060733.4:p.Ala1274Asp
XM_006712039.2:c.3455C>A	XP_006712102.1:p.Ala1152Asp
XM_006712040.1:c.3041C>A	XP_006712103.1:p.Ala1014Asp
XM_011532950.1:c.3818C>A	XP_011531252.1:p.Ala1273Asp
XM_011532951.1:c.3647C>A	XP_011531253.1:p.Ala1216Asp
NM_018263.5:c.3821C>A	NP_060733.4:p.Ala1274Asp
XM_006712039.3:c.3455C>A	XP_006712102.1:p.Ala1152Asp
XM_006712040.2:c.3041C>A	XP_006712103.1:p.Ala1014Asp
XM_011532950.3:c.3818C>A	XP_011531252.1:p.Ala1273Asp
XM_011532951.2:c.3647C>A	XP_011531253.1:p.Ala1216Asp
XM_017004430.1:c.3041C>A	XP_016859919.1:p.Ala1014Asp
XM_024452974.1:c.4001C>A	XP_024308742.1:p.Ala1334Asp
NM_001369346.1:c.3647C>A	NP_001356275.1:p.Ala1216Asp
NM_001369347.1:c.3041C>A	NP_001356276.1:p.Ala1014Asp
NM_018263.6:c.3821C>A MANE Select	NP_060733.4:p.Ala1274Asp