Canonical Allele Identifier: CA346073790

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742190-G-A
• COSMIC: COSM3580265 ; COSM3580266
• MyVariant Identifiers: chr2:g.25965059G>A (hg19) ; chr2:g.25742190G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742190G>A , CM000664.2:g.25742190G>A	GRCh38
NC_000002.11:g.25965059G>A , CM000664.1:g.25965059G>A	GRCh37
NC_000002.10:g.25818563G>A	NCBI36
NG_052995.1:g.141327C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4144C>T	ENSP00000337250.5:p.Pro1382Ser
ENST00000435504.9:c.4147C>T MANE Select	ENSP00000391447.3:p.Pro1383Ser
ENST00000336112.8:c.4063C>T	ENSP00000337250.4:p.Pro1355Ser
ENST00000404843.5:c.2596C>T	ENSP00000383920.1:p.Pro866Ser
ENST00000435504.8:c.4147C>T	ENSP00000391447.3:p.Pro1383Ser
NM_018263.4:c.4147C>T	NP_060733.4:p.Pro1383Ser
XM_006712039.2:c.3781C>T	XP_006712102.1:p.Pro1261Ser
XM_006712040.1:c.3367C>T	XP_006712103.1:p.Pro1123Ser
XM_011532950.1:c.4144C>T	XP_011531252.1:p.Pro1382Ser
XM_011532951.1:c.3973C>T	XP_011531253.1:p.Pro1325Ser
NM_018263.5:c.4147C>T	NP_060733.4:p.Pro1383Ser
XM_006712039.3:c.3781C>T	XP_006712102.1:p.Pro1261Ser
XM_006712040.2:c.3367C>T	XP_006712103.1:p.Pro1123Ser
XM_011532950.3:c.4144C>T	XP_011531252.1:p.Pro1382Ser
XM_011532951.2:c.3973C>T	XP_011531253.1:p.Pro1325Ser
XM_017004430.1:c.3367C>T	XP_016859919.1:p.Pro1123Ser
XM_024452974.1:c.4327C>T	XP_024308742.1:p.Pro1443Ser
NM_001369346.1:c.3973C>T	NP_001356275.1:p.Pro1325Ser
NM_001369347.1:c.3367C>T	NP_001356276.1:p.Pro1123Ser
NM_018263.6:c.4147C>T MANE Select	NP_060733.4:p.Pro1383Ser