Canonical Allele Identifier: CA1557323

Gene: ASXL2

Linked Data

• dbSNP Id: rs765699534
• ExAC: 2:25964927 G / A
• gnomAD v2: 2-25964927-G-A
• gnomAD v3: 2-25742058-G-A
• gnomAD v4: 2-25742058-G-A
• MyVariant Identifiers: chr2:g.25964927G>A (hg19) ; chr2:g.25742058G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742058G>A , CM000664.2:g.25742058G>A	GRCh38
NC_000002.11:g.25964927G>A , CM000664.1:g.25964927G>A	GRCh37
NC_000002.10:g.25818431G>A	NCBI36
NG_052995.1:g.141459C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4276C>T	ENSP00000337250.5:p.Leu1426=
ENST00000435504.9:c.4279C>T MANE Select	ENSP00000391447.3:p.Leu1427=
ENST00000336112.8:c.4195C>T	ENSP00000337250.4:p.Leu1399=
ENST00000404843.5:c.2728C>T	ENSP00000383920.1:p.Leu910=
ENST00000435504.8:c.4279C>T	ENSP00000391447.3:p.Leu1427=
NM_018263.4:c.4279C>T	NP_060733.4:p.Leu1427=
XM_006712039.2:c.3913C>T	XP_006712102.1:p.Leu1305=
XM_006712040.1:c.3499C>T	XP_006712103.1:p.Leu1167=
XM_011532950.1:c.4276C>T	XP_011531252.1:p.Leu1426=
XM_011532951.1:c.4105C>T	XP_011531253.1:p.Leu1369=
NM_018263.5:c.4279C>T	NP_060733.4:p.Leu1427=
XM_006712039.3:c.3913C>T	XP_006712102.1:p.Leu1305=
XM_006712040.2:c.3499C>T	XP_006712103.1:p.Leu1167=
XM_011532950.3:c.4276C>T	XP_011531252.1:p.Leu1426=
XM_011532951.2:c.4105C>T	XP_011531253.1:p.Leu1369=
XM_017004430.1:c.3499C>T	XP_016859919.1:p.Leu1167=
XM_024452974.1:c.4459C>T	XP_024308742.1:p.Leu1487=
NM_001369346.1:c.4105C>T	NP_001356275.1:p.Leu1369=
NM_001369347.1:c.3499C>T	NP_001356276.1:p.Leu1167=
NM_018263.6:c.4279C>T MANE Select	NP_060733.4:p.Leu1427=