Canonical Allele Identifier: CA425354537

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965180_25965185del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742313_25742318del , CM000664.2:g.25742313_25742318del	GRCh38
NC_000002.11:g.25965182_25965187del , CM000664.1:g.25965182_25965187del	GRCh37
NC_000002.10:g.25818686_25818691del	NCBI36
NG_052995.1:g.141201_141206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4018_4023del	ENSP00000337250.5:p.His1340_Asn1341del
ENST00000435504.9:c.4021_4026del MANE Select	ENSP00000391447.3:p.His1341_Asn1342del
ENST00000336112.8:c.3937_3942del	ENSP00000337250.4:p.His1313_Asn1314del
ENST00000404843.5:c.2470_2475del	ENSP00000383920.1:p.His824_Asn825del
ENST00000435504.8:c.4021_4026del	ENSP00000391447.3:p.His1341_Asn1342del
NM_018263.4:c.4021_4026del	NP_060733.4:p.His1341_Asn1342del
XM_006712039.2:c.3655_3660del	XP_006712102.1:p.His1219_Asn1220del
XM_006712040.1:c.3241_3246del	XP_006712103.1:p.His1081_Asn1082del
XM_011532950.1:c.4018_4023del	XP_011531252.1:p.His1340_Asn1341del
XM_011532951.1:c.3847_3852del	XP_011531253.1:p.His1283_Asn1284del
NM_018263.5:c.4021_4026del	NP_060733.4:p.His1341_Asn1342del
XM_006712039.3:c.3655_3660del	XP_006712102.1:p.His1219_Asn1220del
XM_006712040.2:c.3241_3246del	XP_006712103.1:p.His1081_Asn1082del
XM_011532950.3:c.4018_4023del	XP_011531252.1:p.His1340_Asn1341del
XM_011532951.2:c.3847_3852del	XP_011531253.1:p.His1283_Asn1284del
XM_017004430.1:c.3241_3246del	XP_016859919.1:p.His1081_Asn1082del
XM_024452974.1:c.4201_4206del	XP_024308742.1:p.His1401_Asn1402del
NM_001369346.1:c.3847_3852del	NP_001356275.1:p.His1283_Asn1284del
NM_001369347.1:c.3241_3246del	NP_001356276.1:p.His1081_Asn1082del
NM_018263.6:c.4021_4026del MANE Select	NP_060733.4:p.His1341_Asn1342del