Canonical Allele Identifier: CA2658189292

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742076-AATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742082_25742084del , CM000664.2:g.25742082_25742084del	GRCh38
NC_000002.11:g.25964951_25964953del , CM000664.1:g.25964951_25964953del	GRCh37
NC_000002.10:g.25818455_25818457del	NCBI36
NG_052995.1:g.141438_141440del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4255_4257del	ENSP00000337250.5:p.Asp1419del
ENST00000435504.9:c.4258_4260del MANE Select	ENSP00000391447.3:p.Asp1420del
ENST00000336112.8:c.4174_4176del	ENSP00000337250.4:p.Asp1392del
ENST00000404843.5:c.2707_2709del	ENSP00000383920.1:p.Asp903del
ENST00000435504.8:c.4258_4260del	ENSP00000391447.3:p.Asp1420del
NM_018263.4:c.4258_4260del	NP_060733.4:p.Asp1420del
XM_006712039.2:c.3892_3894del	XP_006712102.1:p.Asp1298del
XM_006712040.1:c.3478_3480del	XP_006712103.1:p.Asp1160del
XM_011532950.1:c.4255_4257del	XP_011531252.1:p.Asp1419del
XM_011532951.1:c.4084_4086del	XP_011531253.1:p.Asp1362del
NM_018263.5:c.4258_4260del	NP_060733.4:p.Asp1420del
XM_006712039.3:c.3892_3894del	XP_006712102.1:p.Asp1298del
XM_006712040.2:c.3478_3480del	XP_006712103.1:p.Asp1160del
XM_011532950.3:c.4255_4257del	XP_011531252.1:p.Asp1419del
XM_011532951.2:c.4084_4086del	XP_011531253.1:p.Asp1362del
XM_017004430.1:c.3478_3480del	XP_016859919.1:p.Asp1160del
XM_024452974.1:c.4438_4440del	XP_024308742.1:p.Asp1480del
NM_001369346.1:c.4084_4086del	NP_001356275.1:p.Asp1362del
NM_001369347.1:c.3478_3480del	NP_001356276.1:p.Asp1160del
NM_018263.6:c.4258_4260del MANE Select	NP_060733.4:p.Asp1420del