Canonical Allele Identifier: CA1881474889
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872376_130872384delinsGGTGTGTGC , CM000671.2:g.130872376_130872384delinsGGTGTGTGC GRCh38
NC_000009.11:g.133747763_133747771delinsGGTGTGTGC , CM000671.1:g.133747763_133747771delinsGGTGTGTGC GRCh37
NC_000009.10:g.132737584_132737592delinsGGTGTGTGC NCBI36
NG_012034.1:g.163496_163504delinsGGTGTGTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+163_964+171delinsGGTGTGTGC ENSP00000361423.2:n.964+163_964+171delinsGGTGTGTGC
ENST00000318560.6:c.907+163_907+171delinsGGTGTGTGC MANE Select ENSP00000323315.5:n.907+163_907+171delinsGGTGTGTGC
ENST00000372348.7:c.964+163_964+171delinsGGTGTGTGC ENSP00000361423.2:n.964+163_964+171delinsGGTGTGTGC
ENST00000318560.5:c.907+163_907+171delinsGGTGTGTGC ENSP00000323315.5:n.907+163_907+171delinsGGTGTGTGC
ENST00000372348.6:c.964+163_964+171delinsGGTGTGTGC ENSP00000361423.2:n.964+163_964+171delinsGGTGTGTGC
NM_005157.5:c.907+163_907+171delinsGGTGTGTGC NP_005148.2:n.907+163_907+171delinsGGTGTGTGC
NM_007313.2:c.964+163_964+171delinsGGTGTGTGC NP_009297.2:n.964+163_964+171delinsGGTGTGTGC
NM_005157.6:c.907+163_907+171delinsGGTGTGTGC MANE Select NP_005148.2:n.907+163_907+171delinsGGTGTGTGC
NM_007313.3:c.964+163_964+171delinsGGTGTGTGC NP_009297.2:n.964+163_964+171delinsGGTGTGTGC