Canonical Allele Identifier: CA346073514

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25964936G>A (hg19) ; chr2:g.25742067G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742067G>A , CM000664.2:g.25742067G>A	GRCh38
NC_000002.11:g.25964936G>A , CM000664.1:g.25964936G>A	GRCh37
NC_000002.10:g.25818440G>A	NCBI36
NG_052995.1:g.141450C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4267C>T	ENSP00000337250.5:p.Pro1423Ser
ENST00000435504.9:c.4270C>T MANE Select	ENSP00000391447.3:p.Pro1424Ser
ENST00000336112.8:c.4186C>T	ENSP00000337250.4:p.Pro1396Ser
ENST00000404843.5:c.2719C>T	ENSP00000383920.1:p.Pro907Ser
ENST00000435504.8:c.4270C>T	ENSP00000391447.3:p.Pro1424Ser
NM_018263.4:c.4270C>T	NP_060733.4:p.Pro1424Ser
XM_006712039.2:c.3904C>T	XP_006712102.1:p.Pro1302Ser
XM_006712040.1:c.3490C>T	XP_006712103.1:p.Pro1164Ser
XM_011532950.1:c.4267C>T	XP_011531252.1:p.Pro1423Ser
XM_011532951.1:c.4096C>T	XP_011531253.1:p.Pro1366Ser
NM_018263.5:c.4270C>T	NP_060733.4:p.Pro1424Ser
XM_006712039.3:c.3904C>T	XP_006712102.1:p.Pro1302Ser
XM_006712040.2:c.3490C>T	XP_006712103.1:p.Pro1164Ser
XM_011532950.3:c.4267C>T	XP_011531252.1:p.Pro1423Ser
XM_011532951.2:c.4096C>T	XP_011531253.1:p.Pro1366Ser
XM_017004430.1:c.3490C>T	XP_016859919.1:p.Pro1164Ser
XM_024452974.1:c.4450C>T	XP_024308742.1:p.Pro1484Ser
NM_001369346.1:c.4096C>T	NP_001356275.1:p.Pro1366Ser
NM_001369347.1:c.3490C>T	NP_001356276.1:p.Pro1164Ser
NM_018263.6:c.4270C>T MANE Select	NP_060733.4:p.Pro1424Ser