Canonical Allele Identifier: CA346074983

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742375-G-A
• MyVariant Identifiers: chr2:g.25965244G>A (hg19) ; chr2:g.25742375G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742375G>A , CM000664.2:g.25742375G>A	GRCh38
NC_000002.11:g.25965244G>A , CM000664.1:g.25965244G>A	GRCh37
NC_000002.10:g.25818748G>A	NCBI36
NG_052995.1:g.141142C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3959C>T	ENSP00000337250.5:p.Thr1320Ile
ENST00000435504.9:c.3962C>T MANE Select	ENSP00000391447.3:p.Thr1321Ile
ENST00000336112.8:c.3878C>T	ENSP00000337250.4:p.Thr1293Ile
ENST00000404843.5:c.2411C>T	ENSP00000383920.1:p.Thr804Ile
ENST00000435504.8:c.3962C>T	ENSP00000391447.3:p.Thr1321Ile
NM_018263.4:c.3962C>T	NP_060733.4:p.Thr1321Ile
XM_006712039.2:c.3596C>T	XP_006712102.1:p.Thr1199Ile
XM_006712040.1:c.3182C>T	XP_006712103.1:p.Thr1061Ile
XM_011532950.1:c.3959C>T	XP_011531252.1:p.Thr1320Ile
XM_011532951.1:c.3788C>T	XP_011531253.1:p.Thr1263Ile
NM_018263.5:c.3962C>T	NP_060733.4:p.Thr1321Ile
XM_006712039.3:c.3596C>T	XP_006712102.1:p.Thr1199Ile
XM_006712040.2:c.3182C>T	XP_006712103.1:p.Thr1061Ile
XM_011532950.3:c.3959C>T	XP_011531252.1:p.Thr1320Ile
XM_011532951.2:c.3788C>T	XP_011531253.1:p.Thr1263Ile
XM_017004430.1:c.3182C>T	XP_016859919.1:p.Thr1061Ile
XM_024452974.1:c.4142C>T	XP_024308742.1:p.Thr1381Ile
NM_001369346.1:c.3788C>T	NP_001356275.1:p.Thr1263Ile
NM_001369347.1:c.3182C>T	NP_001356276.1:p.Thr1061Ile
NM_018263.6:c.3962C>T MANE Select	NP_060733.4:p.Thr1321Ile