Canonical Allele Identifier: CA1557339

Gene: ASXL2

Linked Data

• dbSNP Id: rs190294224
• ExAC: 2:25965013 G / A
• gnomAD v2: 2-25965013-G-A
• gnomAD v3: 2-25742144-G-A
• gnomAD v4: 2-25742144-G-A
• MyVariant Identifiers: chr2:g.25965013G>A (hg19) ; chr2:g.25742144G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742144G>A , CM000664.2:g.25742144G>A	GRCh38
NC_000002.11:g.25965013G>A , CM000664.1:g.25965013G>A	GRCh37
NC_000002.10:g.25818517G>A	NCBI36
NG_052995.1:g.141373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4190C>T	ENSP00000337250.5:p.Ser1397Leu
ENST00000435504.9:c.4193C>T MANE Select	ENSP00000391447.3:p.Ser1398Leu
ENST00000336112.8:c.4109C>T	ENSP00000337250.4:p.Ser1370Leu
ENST00000404843.5:c.2642C>T	ENSP00000383920.1:p.Ser881Leu
ENST00000435504.8:c.4193C>T	ENSP00000391447.3:p.Ser1398Leu
NM_018263.4:c.4193C>T	NP_060733.4:p.Ser1398Leu
XM_006712039.2:c.3827C>T	XP_006712102.1:p.Ser1276Leu
XM_006712040.1:c.3413C>T	XP_006712103.1:p.Ser1138Leu
XM_011532950.1:c.4190C>T	XP_011531252.1:p.Ser1397Leu
XM_011532951.1:c.4019C>T	XP_011531253.1:p.Ser1340Leu
NM_018263.5:c.4193C>T	NP_060733.4:p.Ser1398Leu
XM_006712039.3:c.3827C>T	XP_006712102.1:p.Ser1276Leu
XM_006712040.2:c.3413C>T	XP_006712103.1:p.Ser1138Leu
XM_011532950.3:c.4190C>T	XP_011531252.1:p.Ser1397Leu
XM_011532951.2:c.4019C>T	XP_011531253.1:p.Ser1340Leu
XM_017004430.1:c.3413C>T	XP_016859919.1:p.Ser1138Leu
XM_024452974.1:c.4373C>T	XP_024308742.1:p.Ser1458Leu
NM_001369346.1:c.4019C>T	NP_001356275.1:p.Ser1340Leu
NM_001369347.1:c.3413C>T	NP_001356276.1:p.Ser1138Leu
NM_018263.6:c.4193C>T MANE Select	NP_060733.4:p.Ser1398Leu