Canonical Allele Identifier: CA346076046
Gene: ASXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742543A>T , CM000664.2:g.25742543A>T GRCh38
NC_000002.11:g.25965412A>T , CM000664.1:g.25965412A>T GRCh37
NC_000002.10:g.25818916A>T NCBI36
NG_052995.1:g.140974T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.3791T>A ENSP00000337250.5:p.Leu1264Ter
ENST00000435504.9:c.3794T>A MANE Select ENSP00000391447.3:p.Leu1265Ter
ENST00000336112.8:c.3710T>A ENSP00000337250.4:p.Leu1237Ter
ENST00000404843.5:c.2243T>A ENSP00000383920.1:p.Leu748Ter
ENST00000435504.8:c.3794T>A ENSP00000391447.3:p.Leu1265Ter
NM_018263.4:c.3794T>A NP_060733.4:p.Leu1265Ter
XM_006712039.2:c.3428T>A XP_006712102.1:p.Leu1143Ter
XM_006712040.1:c.3014T>A XP_006712103.1:p.Leu1005Ter
XM_011532950.1:c.3791T>A XP_011531252.1:p.Leu1264Ter
XM_011532951.1:c.3620T>A XP_011531253.1:p.Leu1207Ter
NM_018263.5:c.3794T>A NP_060733.4:p.Leu1265Ter
XM_006712039.3:c.3428T>A XP_006712102.1:p.Leu1143Ter
XM_006712040.2:c.3014T>A XP_006712103.1:p.Leu1005Ter
XM_011532950.3:c.3791T>A XP_011531252.1:p.Leu1264Ter
XM_011532951.2:c.3620T>A XP_011531253.1:p.Leu1207Ter
XM_017004430.1:c.3014T>A XP_016859919.1:p.Leu1005Ter
XM_024452974.1:c.3974T>A XP_024308742.1:p.Leu1325Ter
NM_001369346.1:c.3620T>A NP_001356275.1:p.Leu1207Ter
NM_001369347.1:c.3014T>A NP_001356276.1:p.Leu1005Ter
NM_018263.6:c.3794T>A MANE Select NP_060733.4:p.Leu1265Ter