Canonical Allele Identifier: CA1881474927
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872410_130872414delinsTATGA , CM000671.2:g.130872410_130872414delinsTATGA GRCh38
NC_000009.11:g.133747797_133747801delinsTATGA , CM000671.1:g.133747797_133747801delinsTATGA GRCh37
NC_000009.10:g.132737618_132737622delinsTATGA NCBI36
NG_012034.1:g.163530_163534delinsTATGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+197_964+201delinsTATGA ENSP00000361423.2:n.964+197_964+201delinsTATGA
ENST00000318560.6:c.907+197_907+201delinsTATGA MANE Select ENSP00000323315.5:n.907+197_907+201delinsTATGA
ENST00000372348.7:c.964+197_964+201delinsTATGA ENSP00000361423.2:n.964+197_964+201delinsTATGA
ENST00000318560.5:c.907+197_907+201delinsTATGA ENSP00000323315.5:n.907+197_907+201delinsTATGA
ENST00000372348.6:c.964+197_964+201delinsTATGA ENSP00000361423.2:n.964+197_964+201delinsTATGA
NM_005157.5:c.907+197_907+201delinsTATGA NP_005148.2:n.907+197_907+201delinsTATGA
NM_007313.2:c.964+197_964+201delinsTATGA NP_009297.2:n.964+197_964+201delinsTATGA
NM_005157.6:c.907+197_907+201delinsTATGA MANE Select NP_005148.2:n.907+197_907+201delinsTATGA
NM_007313.3:c.964+197_964+201delinsTATGA NP_009297.2:n.964+197_964+201delinsTATGA