Canonical Allele Identifier: CA1881463387
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862943A= , CM000671.2:g.130862943A= GRCh38
NC_000009.11:g.133738330A= , CM000671.1:g.133738330A= GRCh37
NC_000009.10:g.132728151A= NCBI36
NG_012034.1:g.154063A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.787A= ENSP00000361423.2:p.Met263=
ENST00000318560.6:c.730A= MANE Select ENSP00000323315.5:p.Met244=
ENST00000372348.7:c.787A= ENSP00000361423.2:p.Met263=
ENST00000318560.5:c.730A= ENSP00000323315.5:p.Met244=
ENST00000372348.6:c.787A= ENSP00000361423.2:p.Met263=
NM_005157.5:c.730A= NP_005148.2:p.Met244=
NM_007313.2:c.787A= NP_009297.2:p.Met263=
NM_005157.6:c.730A= MANE Select NP_005148.2:p.Met244=
NM_007313.3:c.787A= NP_009297.2:p.Met263=