Canonical Allele Identifier: CA1881474546
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130871958T= , CM000671.2:g.130871958T= GRCh38
NC_000009.11:g.133747345T= , CM000671.1:g.133747345T= GRCh37
NC_000009.10:g.132737166T= NCBI36
NG_012034.1:g.163078T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-171T= ENSP00000361423.2:n.880-171T=
ENST00000318560.6:c.823-171T= MANE Select ENSP00000323315.5:n.823-171T=
ENST00000372348.7:c.880-171T= ENSP00000361423.2:n.880-171T=
ENST00000318560.5:c.823-171T= ENSP00000323315.5:n.823-171T=
ENST00000372348.6:c.880-171T= ENSP00000361423.2:n.880-171T=
NM_005157.5:c.823-171T= NP_005148.2:n.823-171T=
NM_007313.2:c.880-171T= NP_009297.2:n.880-171T=
NM_005157.6:c.823-171T= MANE Select NP_005148.2:n.823-171T=
NM_007313.3:c.880-171T= NP_009297.2:n.880-171T=