Canonical Allele Identifier: CA2576695356
Gene: ASXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742438_25742439insCC , CM000664.2:g.25742438_25742439insCC GRCh38
NC_000002.11:g.25965307_25965308insCC , CM000664.1:g.25965307_25965308insCC GRCh37
NC_000002.10:g.25818811_25818812insCC NCBI36
NG_052995.1:g.141079_141080insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.3896_3897insGG ENSP00000337250.5:p.Ser1299ArgfsTer25
ENST00000435504.9:c.3899_3900insGG MANE Select ENSP00000391447.3:p.Ser1300ArgfsTer25
ENST00000336112.8:c.3815_3816insGG ENSP00000337250.4:p.Ser1272ArgfsTer25
ENST00000404843.5:c.2348_2349insGG ENSP00000383920.1:p.Ser783ArgfsTer25
ENST00000435504.8:c.3899_3900insGG ENSP00000391447.3:p.Ser1300ArgfsTer25
NM_018263.4:c.3899_3900insGG NP_060733.4:p.Ser1300ArgfsTer25
XM_006712039.2:c.3533_3534insGG XP_006712102.1:p.Ser1178ArgfsTer25
XM_006712040.1:c.3119_3120insGG XP_006712103.1:p.Ser1040ArgfsTer25
XM_011532950.1:c.3896_3897insGG XP_011531252.1:p.Ser1299ArgfsTer25
XM_011532951.1:c.3725_3726insGG XP_011531253.1:p.Ser1242ArgfsTer25
NM_018263.5:c.3899_3900insGG NP_060733.4:p.Ser1300ArgfsTer25
XM_006712039.3:c.3533_3534insGG XP_006712102.1:p.Ser1178ArgfsTer25
XM_006712040.2:c.3119_3120insGG XP_006712103.1:p.Ser1040ArgfsTer25
XM_011532950.3:c.3896_3897insGG XP_011531252.1:p.Ser1299ArgfsTer25
XM_011532951.2:c.3725_3726insGG XP_011531253.1:p.Ser1242ArgfsTer25
XM_017004430.1:c.3119_3120insGG XP_016859919.1:p.Ser1040ArgfsTer25
XM_024452974.1:c.4079_4080insGG XP_024308742.1:p.Ser1360ArgfsTer25
NM_001369346.1:c.3725_3726insGG NP_001356275.1:p.Ser1242ArgfsTer25
NM_001369347.1:c.3119_3120insGG NP_001356276.1:p.Ser1040ArgfsTer25
NM_018263.6:c.3899_3900insGG MANE Select NP_060733.4:p.Ser1300ArgfsTer25