Canonical Allele Identifier: CA1881463349
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862929G= , CM000671.2:g.130862929G= GRCh38
NC_000009.11:g.133738316G= , CM000671.1:g.133738316G= GRCh37
NC_000009.10:g.132728137G= NCBI36
NG_012034.1:g.154049G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.773G= ENSP00000361423.2:p.Arg258=
ENST00000318560.6:c.716G= MANE Select ENSP00000323315.5:p.Arg239=
ENST00000372348.7:c.773G= ENSP00000361423.2:p.Arg258=
ENST00000318560.5:c.716G= ENSP00000323315.5:p.Arg239=
ENST00000372348.6:c.773G= ENSP00000361423.2:p.Arg258=
NM_005157.5:c.716G= NP_005148.2:p.Arg239=
NM_007313.2:c.773G= NP_009297.2:p.Arg258=
NM_005157.6:c.716G= MANE Select NP_005148.2:p.Arg239=
NM_007313.3:c.773G= NP_009297.2:p.Arg258=